| type IA |
glycogen storage disease, type I.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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|---|---|
| type IB |
glucose-6-phosphatase translocase deficiency: an autosomal recessive disorder caused by a defect in the transport system for glucose 6-phosphate. Symptoms resemble those of the type I disorder, but patients are additionally predisposed to infection related to neutropenia and to chronic inflammatory bowel disease.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| type II |
lysosomal α-1,4-glucosidase deficiency: an autosomal recessive disorder caused by deficiency of the lysosomal enzyme glucan 1,4-α-glucosidase, with accumulation of glycogen in tissues. In infants, it is characterized by mild hepatomegaly, mental and motor retardation, hypotonia, and cardiomegaly and cardiorespiratory failure resulting in death; the adult form is usually characterized primarily by a gradual skeletal myopathy that sometimes causes respiratory problems.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| type II c.’s |
alveolar c's, type II.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| Type II d. mellitus |
type 2 d. mellitus.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|