医
China Med Service
Best doctors, yours
Breaking down language, channel and process barriers in cross-border care — making the best doctors your personal doctors.
300 Grade-A partner hospitals · 3,000+ leading experts · one-stop service across all specialties
抽风、眼底黄斑部的樱...、肝脾肿大、表情淡漠、短颈、共济失调、腱反射亢进、心动过速、口齿不清、反应迟钝
GM1 gangliosidosis is lysosomal storage disease; beta-galactosidase deficiency; infantile neurodegeneration; cherry-red spot; hepatosplenomegaly; skeletal dysplasia; no cure; palliative.
Developmental regression; cherry-red spot; hepatosplenomegaly; skeletal dysplasia; infantile; hypotonia; no cure
GLB1 mutation; beta-galactosidase deficiency; autosomal recessive; GM1 storage.
Supportive; palliative; enzyme replacement trial; neurology/metabolic; genetic counseling
Pediatrics / neurology / metabolic / genetics.
Warm reminder: Health education reference only; seek care at regular hospital.
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