ROTHMUND-THOMSON SYNDROME-ASSOCIATED WITH ANNULAR PANCREAS AND DUODENAL STENOSIS - A CASE-REPORT

被引：7

作者：

BLAUSTEIN, HS ^{[1
]}

STEVENS, AW ^{[1
]}

STEVENS, PD ^{[1
]}

GROSSMAN, ME ^{[1
]}

机构：

[1] COLUMBIA PRESBYTERIAN MED CTR,DERMATOL CONSULTAT SERV,NEW YORK,NY 10032

来源：

PEDIATRIC DERMATOLOGY | 1993年 / 10卷 / 02期

关键词：

D O I：

10.1111/j.1525-1470.1993.tb00046.x

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

The Rothmund-Thomson syndrome is a rare autosomal recessive condition. It is primarily a clinical diagnosis with manifestations that include polkiloderma, short stature, sparse hair, juvenile cataracts, small hands and feet, bone defects, photosensitivity, hypogonadism, defective dentition, onychodystrophy, and hyperkeratosis. There is only one published case of associated gastrointestinal abnormalities. We report a patient with Rothmund-Thomson syndrome with annular pancreas and duodenal stenosis.

引用

页码：159 / 163

页数：5

共 19 条

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