1) glycogen storage disease Ia
糖原累积病Ⅰa型
2) glycogen storage disease type Ⅲ
糖原累积病Ⅲ型
1.
Recent advances of clinical and genomic study of glycogen storage disease type Ⅲ;
糖原累积病Ⅲ型临床和基因研究进展
3) glycogen storage disease type Ⅱ
Ⅱ型糖原累积病
4) glycogen storage disease
糖原累积病Ⅰ型
1.
Ultrastructural study on live tissue in a case of glycogen storage disease typeⅠ;
糖原累积病Ⅰ型肝脏组织的超微结构观察
5) glycogen storage disease type Ia
Ia型糖原累积病
6) Glycogen storage disease
糖原累积病
1.
Now glycogen storage diseases (GSDs), or glycogenoses, comprise at least 16 subtypes among which McArdle disease(Myophosphorylase deficiency) is an example which invovles muscle only.
目前已知的糖原累积病至少可分为16种类型,McArdle病(肌肉磷酸化酶缺乏症)为少数仅影响肌肉的糖原累积病,有其特征性的临床表现。
补充资料：粘脂质累积病Ⅰ型
粘脂质累积病Ⅰ型
一种常染色体隐性遗传性疾病。骨骼异常进展缓慢，可出现肌张力减低，共济失调及周围神经症状，年长儿可有惊厥，无角膜混浊，周围血淋巴细胞和骨髓细胞有空泡形成或颗粒。肝内β-半乳糖苷酶的活性增高。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条