Suppr超能文献

[Progressive partial lipodystrophy; an external problem with internal anomalies].

作者信息

Hulzebos C V, Bos W H, Doddema J W, van Pinxteren-Nagler E, de Vries T W

机构信息

Afd. Kindergeneeskunde: Medisch Centrum, locatie Noord, Leeuwarden.

出版信息

Ned Tijdschr Geneeskd. 1996 Mar 30;140(13):719-22.

PMID:8668253
Abstract

Progressive partial lipodystrophy (PPL) was diagnosed in two girls aged 6 and 8 years. PPL is characterized by loss of subcutaneous fat, starting in the face and progressing to trunk and arms. Diagnosis is based upon the cachectic appearance and the normal growth parameters. It is a rare disease of unknown aetiology, usually beginning in childhood and more frequent in females. An association with diabetes mellitus, hypertriglyceridaemia and glomerulonephritis has been described. Follow-up should be focused on these and on psychological effects. No causal therapy is available. The facial appearance can be restored by injection of liquid silicones. Life expectancy does not appear to be affected.

摘要

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验