Karande Sunil, Kumbhare Nilesh, Kulkarni Madhuri
Developmental Clinic, Department of Pediatrics, Lokmanya Tilak Municipal Medical College and General Hospital, Sion, Mumbai 400 022, Maharashtra, India.
Indian Pediatr. 2007 Mar;44(3):223-5.
We present here the first case of Fanconi-Bickel syndrome, a rare type of glycogen storage disease, from India. A 17-month-old female child presented with severe growth retardation and abdominal distention. Clinical examination revealed a "doll-like" face, massive hepatomegaly, and rickets. Laboratory investigations confirmed severe hypophosphatemic rickets and proximal renal tubular dysfunction. Liver biopsy showed glycogen accumulation in the hepatocytes.
我们在此报告印度首例范科尼-比克综合征,这是一种罕见的糖原贮积病。一名17个月大的女童出现严重生长发育迟缓及腹胀。临床检查发现其面部呈“娃娃脸”,肝脏肿大明显,并有佝偻病症状。实验室检查确诊为严重低磷性佝偻病及近端肾小管功能障碍。肝脏活检显示肝细胞内有糖原蓄积。