法伯脂肪肉芽肿病：一名黑人儿童的罕见表现。

Farber lipogranulomatosis: an unusual presentation in a black child.

作者信息

Eviatar L, Sklower S L, Wisniewski K, Feldman R S, Gochoco A

机构信息

Department of Pediatric Neurology, Long Island Jewish Medical Center, Schneider Children's Hospital; New Hyde Park, New York 10042.

出版信息

Pediatr Neurol. 1986 Nov-Dec;2(6):371-4. doi: 10.1016/0887-8994(86)90082-2.

DOI:10.1016/0887-8994(86)90082-2

PMID:2854742

Abstract

Farber disease, a rare, inherited condition of lipid metabolism usually appears within the first two months of life. The patients may die in the first few years of life or may live into the second decade. We believe this patient to be the first black American reported with Farber disease. Additionally, the characteristics of the disease in this patient were at variance with previously reported cases.

摘要

法伯病是一种罕见的遗传性脂质代谢疾病，通常在出生后的头两个月内出现。患者可能在生命的最初几年死亡，也可能活到第二个十年。我们认为该患者是首例被报道患有法伯病的美国黑人。此外，该患者的疾病特征与先前报道的病例有所不同。