RAPP-HODGKIN SYNDROME WITH PILI CANALICULI

被引：11

作者：

CAMACHO, F

FERRANDO, J

PICHARDO, AR

SOTILLO, I

JORQUERA, E

机构：

[1] Departments of Medico-Surgical Dermatology Venereology, Barcelona, Sevilla

来源：

PEDIATRIC DERMATOLOGY | 1993年 / 10卷 / 01期

关键词：

D O I：

10.1111/j.1525-1470.1993.tb00015.x

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

A 20-year-old woman and her 12-year-old brother had hypohidrotic ectodermal dysplasia, cleft lip and palate, midfacial hypoplasia with narrow nose from the nasal bridge to the tip, narrow dysplastic nails, and conical teeth and hypodontia, and hypospadias and hypoplastic uvula in the boy. The woman had major underdevelopment of intellectual capacity. The most important hair anomalies in both siblings were sparse eyebrows, pill torti, and pill canaliculi. Some of the pili canaliculi had two canals (pili bicanaliculi), and the cross section for scanning electron microscopy had a quadrangular aspect. This is the seventh family reported with Rapp-Hodgkin ectodermal dysplasia.

引用

页码：54 / 57

页数：4

共 10 条

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