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范科尼-比克综合征

Fanconi-Bickel syndrome.

作者信息

Karande Sunil, Kumbhare Nilesh, Kulkarni Madhuri

机构信息

Developmental Clinic, Department of Pediatrics, Lokmanya Tilak Municipal Medical College and General Hospital, Sion, Mumbai 400 022, Maharashtra, India.

出版信息

Indian Pediatr. 2007 Mar;44(3):223-5.

Abstract

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.

摘要

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。

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