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Glycogénose de type II
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Définition:
An autosomal recessively inherited glycogen storage disease caused by deficiency. Large amounts of accumulate in the of skeletal muscle (); ; ; ; and . Three forms have been described: infantile, childhood, and adult. The infantile form is fatal in infancy and presents with hypotonia and a hypertrophic cardiomyopathy (). The childhood form usually presents in the second year of life with proximal weakness and respiratory symptoms. The adult form consists of a slowly progressive proximal myopathy. (From Muscle Nerve 1995;3:S61-9; Menkes, Textbook of Child Neurology, 5th ed, pp73-4)
Synonyme(s):
Déficit en maltase acide /
GSD II /
Glycogénose de Pompe /
Glycogénose de type 2 /
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(NLM)®
de l'INSERM (version française)
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