公开概念 · 1e1ab1f6-0ea6-4b7b-94e3-b54d35fd34e7
杜兴氏肌肉营养不良症
英语
en
DMD认可
Duchenne muscular dystrophy首选
“A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy.”
Duchenne-type muscular dystrophy认可
severe dystrophinopathy认可
中文(中国)
zh-CN
杜兴氏肌肉营养不良症首选