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  • Picmonic Glycogen Storage Diseases

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    Laylee Clare
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    Glycogen storage diseases are a group of metabolic disorders caused by defects in glycogen breakdown in the liver or muscle. Type I (von Gierke disease) is caused by a deficiency of glucose-6-phosphatase and results in an accumulation of glycogen and fat in the liver and kidneys. Type II (Pompe disease) is caused by a deficiency of acid alpha-glucosidase and results in glycogen buildup in muscles throughout the body. Type III (Cori disease) is caused by a deficiency of debranching enzyme and results in glycogen accumulation in the liver and muscle.

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    Glycogen storage diseases are a group of metabolic disorders caused by defects in glycogen breakdown in the liver or muscle. Type I (von Gierke disease) is caused by a deficiency of glucose-6-phosphatase and results in an accumulation of glycogen and fat in the liver and kidneys. Type II (Pompe disease) is caused by a deficiency of acid alpha-glucosidase and results in glycogen buildup in muscles throughout the body. Type III (Cori disease) is caused by a deficiency of debranching enzyme and results in glycogen accumulation in the liver and muscle.

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    2K visualizzazioni2 pagine

    Picmonic Glycogen Storage Diseases

    Caricato da

    Laylee Clare
    Glycogen storage diseases are a group of metabolic disorders caused by defects in glycogen breakdown in the liver or muscle. Type I (von Gierke disease) is caused by a deficiency of glucose-6-phosphatase and results in an accumulation of glycogen and fat in the liver and kidneys. Type II (Pompe disease) is caused by a deficiency of acid alpha-glucosidase and results in glycogen buildup in muscles throughout the body. Type III (Cori disease) is caused by a deficiency of debranching enzyme and results in glycogen accumulation in the liver and muscle.

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    © All Rights Reserved
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    di 2

    Glycogen Storage Diseases

    Von Gierke Disease (Type I)

    Pompe Disease (Type II)

    Cori Disease (Type III)


    McArdle Disease (Type V)

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