Documenti di Didattica
Documenti di Professioni
Documenti di Cultura
6/28/15, 6:38
Nephrotic syndrome
From Wikipedia, the free encyclopedia
Nephrotic syndrome
edema.[1]
N04
(http://apps.who.int/classifications/icd10/browse/2015/en#/N04)
ICD-9
581 (http://www.icd9data.com/getICD9Code.ashx?icd9=581)
med/1612 (http://www.emedicine.com/med/topic1612.htm)
ped/1564 (http://www.emedicine.com/ped/topic1564.htm#)
MeSH
D009404 (https://www.nlm.nih.gov/cgi/mesh/2015/MB_cgi?
field=uid&term=D009404)
Contents
1 Signs and symptoms
1.1 Clinical symptoms
2 Pathophysiology
3 Causes and classification
3.1 Primary glomerulonephritis
3.2 Secondary glomerulonephritis
3.2.1 Secondary causes by histologic pattern
4 Diagnosis
4.1 Classification
4.2 Differential diagnosis
5 Complications
6 Treatment
6.1 Symptomatic treatment
6.2 Treatment of kidney damage
7 Epidemiology
8 Prognosis
https://en.wikipedia.org/wiki/Nephrotic_syndrome
Page 1 of 12
6/28/15, 6:38
9 See also
10 References
11 External links
Clinical symptoms
The main symptoms of nephrotic syndrome are:[6]
A proteinuria of greater than 3.5 g /24 h /1.73 m s or 40 mg/h/m2 in children (between 3 and 3.5 g/24 h is considered to be
proteinuria in the nephrotic range).[7][8] The ratio between urinary concentrations of albumin and creatinin can be used in
the absence of a 24-hour urine test for total protein. This coefficient will be greater than 200400 mg/mmol in nephrotic
syndrome. This pronounced loss of proteins is due to an increase in glomerular permeability that allows proteins to pass
into the urine instead of being retained in the blood. Under normal conditions a 24-hour urine sample should not exceed 80
milligrams or 10 milligrams per decilitre.[9]
A hypoalbuminemia of less than 2.5 g/dL,[7] that exceeds the hepatic clearance level, that is, protein synthesis in the liver
is insufficient to increase the low blood protein levels.
Edema is thought to be caused by two mechanisms. The first being hypoalbuminemia which lowers the oncotic pressure
within vessels resulting in hypovolemia and subsequent activation of the Renin-angiotensin system and thus retention of
sodium and water. Additionally, it is thought that albumin causes a direct effect on the epithelial sodium channel (ENaC) on
https://en.wikipedia.org/wiki/Nephrotic_syndrome
Page 2 of 12
the principal cell that leads to the reabsorption of sodium and water. Nephrotic
syndrome edema initially appears in parts of the lower body (such as the legs)
and in the eyelids. In the advanced stages it also extends to the pleural cavity and
peritoneum (ascites) and can even develop into a generalized anasarca. It has
been recently seen that intrarenal sodium handling abnormality is related to Atrial
Natriuretic Peptide resistance is associated with decreased abundance and altered
subcellular localization of dopamine receptor in renal tubules.[10]
Hyperlipidaemia is caused by an increase in the synthesis of low and very lowdensity lipoproteins in the liver that are responsible for the transport of
cholesterol and triglycerides. There is also an increase in the hepatic synthesis of
cholesterol.
Thrombophilia, or hypercoagulability, is a greater predisposition for the
formation of blood clots that is caused by a decrease in the levels of antithrombin
III in the blood due to its loss in urine.
Lipiduria or loss of lipids in the urine is indicative of glomerular pathology due to
an increase in the filtration of lipoproteins.[11]
6/28/15, 6:38
Pathophysiology
The renal glomerulus filters the blood that arrives at the kidney. It is formed of capillaries with small
pores that allow small molecules to pass through that have a molecular weight of less than 40,000
Daltons,[12] but not larger macromolecules such as proteins.
In nephrotic syndrome, the glomeruli are affected by an inflammation or a hyalinization (the
formation of a homogenous crystalline material within cells) that allows proteins such as albumin,
antithrombin or the immunoglobulins to pass through the cell membrane and appear in urine.[13]
Albumin is the main protein in the blood that is able to maintain an oncotic pressure, which prevents
the leakage of fluid into the extracellular medium and the subsequent formation of edemas.
As a response to hypoproteinemia the liver commences a compensatory mechanism involving the
synthesis of proteins, such as alpha-2 macroglobulin and lipoproteins.[13] An increase in the latter
can cause the hyperlipidemia associated with this syndrome.
Primary glomerulonephritis
Primary causes of nephrotic syndrome are usually described by their histology:[14]
Minimal change disease (MCD): is the most common cause of nephrotic
Histological image of a normal kidney
syndrome in children. It owes its name to the fact that the nephrons appear
normal when viewed with an optical microscope as the lesions are only visible
glomerulus. It is possible to see a
using an electron microscope. Another symptom is a pronounced proteinuria.
glomerulus in the centre of the image
Focal segmental glomerulosclerosis (FSGS): is the most common cause of
surrounded by renal tubules.
nephrotic syndrome in adults.[15] It is characterized by the appearance of tissue
scarring in the glomeruli. The term focal is used as some of the glomeruli have scars, while others appear intact; the term
segmental refers to the fact that only part of the glomerulus suffers the damage.
https://en.wikipedia.org/wiki/Nephrotic_syndrome
Page 3 of 12
6/28/15, 6:38
Membranous glomerulonephritis (IMN): The inflammation of the glomerular membrane causes increased leaking in the
kidney. It is not clear why this condition develops in most people, although an auto-immune mechanism is suspected.[15]
Mesangial proliferative glomerulonephritis (MPGN): is the inflammation of the glomeruli along with the deposit of
antibodies in their membranes, which makes filtration difficult.
Rapidly progressive glomerulonephritis (RPGN): (Usually presents as a nephritic syndrome) A patients glomeruli are
present in a crescent moon shape. It is characterized clinically by a rapid decrease in the glomerular filtration rate (GFR) by
at least 50% over a short period, usually from a few days to 3 months.[16]
They are considered to be "diagnoses of exclusion", i.e. they are diagnosed only after secondary causes have been excluded.
Secondary glomerulonephritis
Secondary causes of nephrotic syndrome have the same histologic patterns as the
primary causes, though they may exhibit some difference suggesting a secondary cause,
such as inclusion bodies.[17] They are usually described by the underlying cause.
Diabetic nephropathy: is a complication that occurs in some diabetics. Excess
blood sugar accumulates in the kidney causing them to become inflamed and
unable to carry out their normal function. This leads to the leakage of proteins
into the urine.
Systemic lupus erythematosus: this autoimmune disease can affect a number of
organs, among them the kidney, due to the deposit of immunocomplexes that are
typical to this disease. The disease can also cause lupus nephritis.
Diabetic glomerulonephritis in a patient
Sarcoidosis: This disease does not usually affect the kidney but, on occasions, the
with nephrotic syndrome.
accumulation of inflammatory granulomas (collection of immune cells) in the
glomeruli can lead to nephrotic syndrome.
Syphilis: kidney damage can occur during the secondary stage of this disease (between 2 and 8 weeks from onset).
Hepatitis B: certain antigens present during hepatitis can accumulate in the kidneys and damage them.
Sjgren's syndrome: this autoimmune disease causes the deposit of immunocomplexes in the glomeruli, causing them to
become inflamed, this is the same mechanism as occurs in systemic lupus erythematosus.
HIV: the virus antigens provoke an obstruction in the glomerular capillarys lumen that alters normal kidney function.
Amyloidosis: the deposit of amyloid substances (proteins with anomalous structures) in the glomeruli modifying their
shape and function.
Multiple myeloma: the cancerous cells arrive at the kidney causing glomerulonephritis as a complication.
Vasculitis: inflammation of the blood vessels at a glomerular level impedes the normal blood flow and damages the kidney.
Cancer: as happens in myeloma, the invasion of the glomeruli by cancerous cells disturbs their normal functioning.
Genetic disorders: congenital nephrotic syndrome is a rare genetic disorder in which the protein nephrin, a component of
the glomerular filtration barrier, is altered.
Drugs ( e.g. gold salts, penicillin, captopril):[18] gold salts can cause a more or less important loss of proteins in urine as a
consequence of metal accumulation. Penicillin is nephrotoxic in patients with kidney failure and captopril can aggravate
proteinuria.
Secondary causes by histologic pattern
Membranous nephropathy (MN)
Sjgren's syndrome
Systemic lupus erythematosus (SLE)
Diabetes mellitus
Sarcoidosis
Drugs (such as corticosteroids, gold, intravenous heroin)
Malignancy (cancer)
Bacterial infections, e.g. leprosy & syphilis
Protozoal infections, e.g. malaria
https://en.wikipedia.org/wiki/Nephrotic_syndrome
Page 4 of 12
6/28/15, 6:38
Diagnosis
Along with obtaining a complete medical history, a series of biochemical tests are required in
order to arrive at an accurate diagnosis that verifies the presence of the illness. In addition,
imaging of the kidneys (for structure and presence of two kidneys) is sometimes carried out,
and/or a biopsy of the kidneys. The first test will be a urinalysis to test for high levels of
proteins,[21] as a healthy subject excretes an insignificant amount of protein in their urine.
The test will involve a 24-hour bedside urinary total protein estimation. The urine sample is
tested for proteinuria (>3.5 g per 1.73 m2 per 24 hours). It is also examined for urinary casts,
which are more a feature of active nephritis. Next a blood screen, comprehensive metabolic
panel (CMP) will look for hypoalbuminemia: albumin levels of 2.5 g/dL (normal=3.5-5
g/dL). Then a Creatinine Clearance CCr test will evaluate renal function particularly the
glomerular filtration capacity.[22] Creatinine formation is a result of the breakdown of
muscular tissue, it is transported in the blood and eliminated in urine. Measuring the
concentration of organic compounds in both liquids evaluates the capacity of the glomeruli to
filter blood. Electrolytes and urea levels may also be analysed at the same time as creatinine
(EUC test) in order to evaluate renal function. A lipid profile will also be carried out as high
levels of cholesterol (hypercholesterolemia), specifically elevated LDL, usually with
concomitantly elevated VLDL, is indicative of nephrotic syndrome.
A kidney biopsy may also be used as a more specific and invasive test method. A study of a samples anatomical pathology may
then allow the identification of the type of glomerulonephritis involved.[21] However, this procedure is usually reserved for adults
as the majority of children suffer from minimum change disease that has a remission rate of 95% with corticosteroids.[23] A
biopsy is usually only indicated for children that are corticosteroid resistant as the majority suffer from focal and segmental
glomeruloesclerosis.[23]
Further investigations are indicated if the cause is not clear including analysis of auto-immune markers (ANA, ASOT, C3,
cryoglobulins, serum electrophoresis), or ultrasound of the whole abdomen.
Classification
A broad classification of nephrotic syndrome based on underlying cause:
Nephrotic
syndrome
https://en.wikipedia.org/wiki/Nephrotic_syndrome
Page 5 of 12
6/28/15, 6:38
Primary
Secondary
MCD
FSGS
MN
MPGN
Differential diagnosis
Some symptoms that are present in nephrotic syndrome, such as edema and proteinuria, also appear in other illnesses. Therefore,
other pathologies need to be excluded in order to arrive at a definitive diagnosis.[24]
Edema: in addition to nephrotic syndrome there are two other disorders that often present with edema; these are heart
failure and liver failure.[25] Congestive heart failure can cause liquid retention in tissues as a consequence of the decrease in
the strength of ventricular contractions. The liquid is initially concentrated in the ankles but it subsequently becomes
generalized and is called anasarca.[26] Patients with congestive heart failure also experience an abnormal swelling of the
heart cardiomegaly, which aids in making a correct diagnosis. Jugular venous pressure can also be elevated and it might be
possible to hear heart murmurs. An echocardiogram is the preferred investigation method for these symptoms. Liver failure
caused by cirrhosis, hepatitis and other conditions such as alcoholism, IV drug use or some hereditary diseases can lead to
swelling in the lower extremities and the abdominal cavity. Other accompanying symptoms include jaundice, dilated veins
over umbilicus (caput medusae), scratch marks (due to widespread itching, known as pruritus), enlarged spleen, spider
angiomata, encephalopathy, bruising, nodular liver and anomalies in the liver function tests.[27] Less frequently symptoms
associated with the administration of certain pharmaceutical drugs have to be discounted. These drugs promote the
retention of liquid in the extremities such as occurs with NSAIs, some antihypertensive drugs, the adrenal corticosteroids
and sex hormones.[27]
Acute fluid overload can cause edema in someone with kidney failure. These people are known to have kidney failure, and have
either drunk too much or missed their dialysis. In addition, when Metastatic cancer spreads to the lungs or abdomen it causes
effusions and fluid accumulation due to obstruction of lymphatic vessels and veins, as well as serous exudation.
Proteinuria: the loss of proteins from the urine is caused by many pathological agents and infection by these agents has to
be ruled out before it can be certain that a patient has nephrotic syndrome. Multiple myeloma can cause a proteinuria that is
not accompanied by hypoalbuminemia, which is an important aid in making a differential diagnosis;[28] other potential
causes of proteinuria include asthenia, weight loss or bone pain. In diabetes mellitus there is an association between
increases in glycated hemoglobin levels and the appearance of proteinuria.[29] Other causes are amyloidosis and certain
other allergic and infectious diseases.
Complications
Nephrotic syndrome can be associated with a series of complications that can affect an individuals health and quality of life:[13]
Thromboembolic disorders: particularly those caused by a decrease in blood antithrombin III levels due to leakage.
Antithrombin III counteracts the action of thrombin. Thrombosis usually occurs in the renal veins although it can also
occur in arteries. Treatment is with oral anticoagulants (not heparin as heparin acts via anti-thrombin 3 which is lost in the
https://en.wikipedia.org/wiki/Nephrotic_syndrome
Page 6 of 12
6/28/15, 6:38
proteinuria so it will be ineffective.) Hypercoagulopathy due to extravasation of fluid from the blood vessels (edema) is
also a risk for venous thrombosis.
Infections: The increased susceptibility of patients to infections can be a result of the leakage of immunoglobulins from the
blood, the loss of proteins in general and the presence of oedematous fluid (which acts as a breeding ground for infections).
The most common infection is peritonitis, followed by lung, skin and urinary infections, meningoencephalitis and in the
most serious cases septicaemia. The most notable of the causative organisms are Streptococcus pneumoniae and
Haemophilus influenzae.
Acute kidney failure due to hypovolemia: the loss of vascular fluid into the tissues (edema) produces a decreased blood
supply to the kidneys that causes a loss of kidney function. Thus it is a tricky task to get rid of excess fluid in the body
while maintaining circulatory euvolemia.
Pulmonary edema: the loss of proteins from blood plasma and the consequent fall in oncotic pressure causes an abnormal
accumulation of liquid in the lungs causing hypoxia and dyspnoea.
Hypothyroidism: deficiency of the thyroglobulin transport protein thyroxin (a glycoprotein that is rich in iodine and is
found in the thyroid gland) due to decreased thyroid binding globulin.
Hypocalcaemia: lack of 25-hydroxycholecalciferol (the way that vitamin D is stored in the body). As vitamin D regulates
the amount of calcium present in the blood a decrease in its concentration will lead to a decrease in blood calcium levels. It
may be significant enough to cause tetany. Hypocalcaemia may be relative; calcium levels should be adjusted based on the
albumin level and ionized calcium levels should be checked.
Microcytic hypochromic anaemia: iron deficiency caused by the loss of ferritin (compound used to store iron in the body).
It is iron-therapy resistant.
Protein malnutrition: this occurs when the amount of protein that is lost in the urine is greater than that ingested, this leads
to a negative nitrogen balance.[30][31]
Growth retardation: can occur in cases of relapse or resistance to therapy. Causes of growth retardation are protein
deficiency from the loss of protein in urine, anorexia (reduced protein intake), and steroid therapy (catabolism).
Vitamin D deficiency can occur. Vitamin D binding protein is lost.
Cushing's Syndrome
Treatment
The treatment of nephrotic syndrome can be symptomatic or can directly address the injuries caused to the kidney.
Symptomatic treatment
The objective of this treatment is to treat the imbalances brought about by the illness:[32] edema, hypoalbuminemia, hyperlipemia,
hypercoagulability and infectious complications.
Edema: a return to an unswollen state is the prime objective of this treatment of nephrotic syndrome. It is carried out
through the combination of a number of recommendations:
Rest: depending on the seriousness of the edema and taking into account the risk of thrombosis caused by prolonged
bed rest.[33]
Medical nutrition therapy: based on a diet with the correct energy intake and balance of proteins that will be used in
synthesis processes and not as a source of calories. A total of 35 kcal/kg body weight/day is normally
recommended.[34] This diet should also comply with two more requirements: the first is to not consume more than 1
g of protein/kg body weight/ day,[34] as a greater amount could increase the degree of proteinuria and cause a
negative nitrogen balance.[31] Patients are usually recommended lean cuts of meat, fish, and poultry. The second
guideline requires that the amount of water ingested is not greater than the level of diuresis. In order to facilitate this
the consumption of salt must also be controlled, as this contributes to water retention. It is advisable to restrict the
ingestion of sodium to 1 or 2 g/day, which means that salt cannot be used in cooking and salty foods should also be
avoided.[35] Foods high in sodium include seasoning blends (garlic salt, Adobo, season salt, etc.) canned soups,
canned vegetables containing salt, luncheon meats including turkey, ham, bologna, and salami, prepared foods, fast
foods, soy sauce, ketchup, and salad dressings. On food labels, compare milligrams of sodium to calories per serving.
https://en.wikipedia.org/wiki/Nephrotic_syndrome
Page 7 of 12
6/28/15, 6:38
When the thrombophilia is such that it leads to the formation of blood clots, heparin is given for at least 5 days along with
oral anticoagulants (OAC). During this time and if the prothrombin time is within its therapeutic range (between 2 and 3),[42] it
may be possible to suspend the LMWH while maintaining the OACs for at least 6 months.[43]
Infectious complications: an appropriate course of antibacterial drugs can be taken according to the infectious agent.
In addition to these key imbalances, vitamin D and calcium are also taken orally in case the alteration of vitamin D causes a
severe hypocalcaemia, this treatment has the goal of restoring physiological levels of calcium in the patient.[44]
Achieving better blood glucose level control if the patient is diabetic.
Blood pressure control. ACE inhibitors are the drug of choice. Independent of their blood pressure lowering effect, they
have been shown to decrease protein loss.
Page 8 of 12
6/28/15, 6:38
negative test for proteinuria in three urine samples taken during the night.
Corticosteroid resistant patient or late steroid-responder: the proteinuria persists after the 8-week treatment. The lack
of response is indicative of the seriousness of the glomerular damage, which could develop into chronic kidney
failure.
Corticosteroid tolerant patient: complications such as hypertension appear, patients gain a lot of weight and can
develop aseptic or avascular necrosis of the hip or knee,[46] cataracts and thrombotic phenomena and/or embolisms.
Corticosteroid dependent patient: proteinuria appears when the dose of corticosteroid is decreased or there is a
relapse in the first two weeks after treatment is completed.
Immunosupressors (cyclophosphamide): only indicated in recurring nephrotic syndrome in corticosteroid dependent or
intolerant patients. In the first two cases the proteinuria has to be negated before treatment with the immunosuppressor can
begin, which involves a prolonged treatment with prednisone. The negation of the proteinuria indicates the exact moment
when treatment with cyclophosphamide can begin. The treatment is continued for 8 weeks at a dose of 3 mg/kg/day, the
immunosuppression is halted after this period. In order to be able to start this treatment the patient should not be suffering
from neutropenia nor anaemia, which would cause further complications. A possible side effect of the cyclophosphamide is
alopecia. Complete blood count tests are carried out during the treatment in order to give advance warning of a possible
infection.
Epidemiology
Nephrotic syndrome can affect any age, although it is mainly found in adults with a ratio of adults to children of 26 to 1.[47]
The syndrome presents in different ways in the two groups: the most frequent glomerulopathy in children is minimal change
disease (66% of cases), followed by focal and segmental glomeruloesclerosis (8%) and mesangiocapillary glomerulonephritis
(6%).[17] In adults the most common disease is mesangiocapillary glomerulonephritis (30-40%), followed by focal and segmental
glomeruloesclerosis (15-25%) and minimal change disease (20%). The latter usually presents as secondary and not primary as
occurs in children. Its main cause is diabetic nephropathy.[17] It usually presents in a patients 40s or 50s. Of the
glomerulonephritis cases approximately 60% to 80% are primary, while the remainder are secondary.[47]
There are also differences in epidemiology between the sexes, the disease is more common in men than in women by a ratio of 2
to 1.[47]
The epidemiological data also reveals information regarding the most common way that symptoms develop in patients with
nephrotic syndrome:[47] spontaneous remission occurs in up to 20% or 30% of cases during the first year of the illness. However,
this improvement is not definitive as some 50% to 60% of patients die and / or develop chronic renal failure 6 to 14 years after
this remission. On the other hand, between 10% and 20% of patients have continuous episodes of remissions and relapses without
dying or jeopardizing their kidney. The main causes of death are cardiovascular, as a result of the chronicity of the syndrome, and
thromboembolic accidents.
Prognosis
The prognosis for nephrotic syndrome under treatment is generally good although this depends on the underlying cause, the age
of the patient and their response to treatment. It is usually good in children, because minimal change disease responds very well
to steroids and does not cause chronic renal failure. Any relapses that occur become less frequent over time;[48] the opposite
occurs with mesangiocapillary glomerulonephritis, in which the kidney fails within three years of the disease developing, making
dialysis necessary and subsequent kidney transplant.[48] In addition children under the age of 5 generally have a poorer prognosis
than prepubescents, as do adults older than 30 years of age as they have a greater risk of kidney failure.[49]
Other causes such as focal segmental glomerulosclerosis frequently lead to end stage renal disease. Factors associated with a
poorer prognosis in these cases include level of proteinuria, blood pressure control and kidney function (GFR).
https://en.wikipedia.org/wiki/Nephrotic_syndrome
Page 9 of 12
6/28/15, 6:38
Without treatment nephrotic syndrome has a very bad prognosis especially rapidly progressing glomerulonephritis, which leads
to acute kidney failure after a few months.
See also
Lipiduria
Nephritic syndrome
Low-dose naltrexone
References
1. http://wordnetweb.princeton.edu/perl/webwn?s=nephrotic%20syndrome
2. "ELECTRONIC LEARNING MODULE for KIDNEY and URINARY TRACT DISEASES"
(http://www.som.tulane.edu/classware/pathology/medical_pathology/New_for_2001/renal/chap7.html). Retrieved 2008-11-26.
3. http://www.hawaii.edu/medicine/pediatrics/pedtext/s13c02.html
4. Freedberg, Irwin M. et.al, ed. (2003). Fitzpatrick's dermatology in general medicine. (6th ed.). New York, NY [u.a.]: McGraw-Hill. p. 659.
ISBN 0-07-138076-0.
5. Behrman, Richard E.; Robert M Kliegman; Hal B. Jenson (2008). Nelson Tratado de Pediatria (in Spanish). Elsevier, Espaa. p. 1755.
ISBN 8481747475.
6. "Manifestaciones clnicas del sndrome nefrtico"
(http://www.saber.ula.ve/db/ssaber/Edocs/grupos/nefrologia/publicaciones/monografias/compendio/e-capitulo4.pdf) (PDF). See table 4.2.
Retrieved 12-09-2008. Check date values in: |accessdate= (help)
7. Garca - Conde, J.; Merino Snchez, J.; Gonzlez Macas, J. (1995). "Fisiopatologa glomerular". Patologa General. Semiologa Clnica y
Fisiopatologa. McGraw - Hill Interamericana. ISBN 8448600932.
8. Parra Herrn, Carlos Eduardo; Castillo Londoo, Juan Sebastin; Lpez Panqueva, Roco del Pilar; Andrade Prez, Rafael Enrique.
"Sndrome nefrtico y proteinuria en rango no nefrtico" (http://patologia.es/volumen39/vol39-num4/39-4n05.htm). Retrieved 2008-09-14.
9. "Valores normales de protena en orina de 24 horas" (http://www.nlm.nih.gov/medlineplus/spanish/ency/article/003622.htm). Retrieved
24 August 2012.
10. Ctia Fernandes-Cerqueira, Benedita Sampaio-Maia, Janete Quelhas-Santos, Mnica Moreira-Rodrigues, Liliana Simes-Silva, Ana M.
Blazquez-Medela, C. Martinez-Salgado, Jose M. Lopez-Novoa, and Manuel Pestana (2013). "Concerted Action of ANP and Dopamine D1Receptor to Regulate Sodium Homeostasis in Nephrotic Syndrome" (http://www.hindawi.com/journals/bmri/2013/397391/). BioMed
Research International 2013 (397391). doi:10.1155/2013/397391 (https://dx.doi.org/10.1155%2F2013%2F397391). PMC 3727124
(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3727124). PMID 23956981 (https://www.ncbi.nlm.nih.gov/pubmed/23956981).
11. "La prdida de lipoprotenas en la orina" (http://66.102.9.132/search?
q=cache:5pmFposW3C8J:www.semiologiaclinica.com/Images/nefrotico.doc). Retrieved 2008-11-21.
12. "Apuntes de fisiopatologa de sistemas" (http://escuela.med.puc.cl/paginas/cursos/tercero/IntegradoTercero/Mec231_38.html). Retrieved 0809-2008. Check date values in: |accessdate= (help)
13. Durn lvarez, Sandalio. "Complicaciones agudas del sndrome nefrtico" (http://scielo.sld.cu/scielo.php?script=sci_arttext&pid=S003475311999000400010). Retrieved 11-09-2008. Check date values in: |accessdate= (help)
14. "Descripcin histolgica de las glomerulonefritis ideopticas" (http://www.senefro.org/modules.php?
name=subsection&idsection=3&idsubsection=264). Retrieved 08-09-2008. Check date values in: |accessdate= (help)
15. "Patient information: The nephrotic syndrome (Beyond the Basics)" (http://www.uptodate.com/contents/the-nephrotic-syndrome-beyond-thebasics). Retrieved 2013-06-28.
16. James W Lohr, MD. "Rapidly progressive glomerulonephritis" (http://emedicine.medscape.com/article/240457-overview). Retrieved
2013-06-28.
17. "Frecuencia de las glomerulonefritis y causas de las glomerulonefritis secundarias" (http://webcache.googleusercontent.com/search?
q=cache:hsqMptZ7b3AJ:sabanet.unisabana.edu.co/medicina/semestre7/medinterna_I/guis20052/SINDROMES%2520GLOMERULARES%25202.doc). Retrieved 08-09-2008. Check date values in: |accessdate= (help)
18. "Frmacos que pueden producir sndrome nefrtico" (http://www.cepvi.com/medicina/enfermedades/sindrome_nefrotico4.shtml). Retrieved
08-09-2008. Check date values in: |accessdate= (help)
19. Fogo AB, Bruijn JA. Cohen AH, Colvin RB, Jennette JC. Fundamentals of Renal Pathology. Springer. ISBN 978-0-387-31126-5.
20. "Nephrotic syndrome" (https://www.clinicalkey.com/topics/nephrology/nephrotic-syndrome.html). Retrieved 08-06-2013. Check date values
in: |accessdate= (help)
21. "Nefrologa y urologa" (http://www.mapfre.es/salud/es/cinformativo/sindrome-nefrotico.shtml). Retrieved 12-09-2008. Check date values
in: |accessdate= (help)
22. "El diagnstico del sndrome nefrtico" (http://www.urovirtual.net/paciente/saber/rinyones/articulo9.asp). Retrieved 12-09-2008. Check date
values in: |accessdate= (help)
23. Voguel S, Andrea; Azcar P, Marta; Nazal Ch, Vilma; Salas del C, Paulina. "Indicaciones de la biospsia renal en nios"
(http://www.scielo.cl/scielo.php?pid=S0370-41062006000300011&script=sci_arttext). Retrieved 2008-09-14.
https://en.wikipedia.org/wiki/Nephrotic_syndrome
Page 10 of 12
6/28/15, 6:38
External links
Nephrotic Syndrome Research (http://www.fsgs.bwh.harvard.edu) A team of kidney doctors and scientists from Beth Israel
Deaconess Medical Center / Harvard Medical School working to learn more about the cause of Nephrotic Syndrome in
https://en.wikipedia.org/wiki/Nephrotic_syndrome
Page 11 of 12
6/28/15, 6:38
children and adults, with an emphasis on the genetic basis of this disease.
Childhood Nephrotic Syndrome (http://kidney.niddk.nih.gov/kudiseases/pubs/childhoodnephrotic/) - National Institute of
Diabetes and Digestive and Kidney Diseases (NIDDK), NIH
Adult Nephrotic Syndrome (http://kidney.niddk.nih.gov/kudiseases/pubs/nephrotic/) - National Institute of Diabetes and
Digestive and Kidney Diseases (NIDDK), NIH
Kidcomm.org A resource for parents of children with nephrotic syndrome since 2007 (http://www.kidcomm.org/)
Clardy, Chris (May 2000) "Nephrotic Syndrome in Children
(http://pediatrics.uchicago.edu/chiefs/nephro/documents/Peds_Nephro_for_Residents_Nov2005.pdf)" Pediatric
Nephrology Handout
Goldstein, Adam; Trachtman, Howard "Pediatric Nephrotic Syndrome
(http://www.kidney.org/site/107/pdf/NephroticSyndrome.pdf)"
Nephrotic syndrome - Medline Plus (http://www.nlm.nih.gov/medlineplus/ency/article/000490.htm)
Retrieved from "https://en.wikipedia.org/w/index.php?title=Nephrotic_syndrome&oldid=667998264"
Categories: Kidney diseases Pediatrics Syndromes
This page was last modified on 21 June 2015, at 21:39.
Text is available under the Creative Commons Attribution-ShareAlike License; additional terms may apply. By using this
site, you agree to the Terms of Use and Privacy Policy. Wikipedia is a registered trademark of the Wikimedia Foundation,
Inc., a non-profit organization.
https://en.wikipedia.org/wiki/Nephrotic_syndrome
Page 12 of 12