A newly recognized syndrome with double upper and lower lip, hypertelorism, eyelid ptosis, blepharophimosis, and third finger clinodactyly

被引：12

作者：

Parmar, RC

Muranjan, MN

机构：

[1] Seth GS Med Coll, Dept Pediat, Div Genet, Bombay, Maharashtra, India

[2] King Edward Mem Hosp, Bombay, Maharashtra, India

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 2004年 / 124A卷 / 02期

关键词：

Ascher syndrome;

D O I：

10.1002/ajmg.a.20313

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

Congenital double lip is an uncommon developmental abnormality usually affecting the upper lip. We report a 21-year-old male with double upper and lower lip, hypertelorism, unilateral ptosis, blepharophimosis, and broad nose with broad nasal tip, highly arched palate, and bilateral third finger clinodactyly. The disorder differs from Ascher syndrome and appears to represent a newly recognized syndrome. (C) 2003 Wiley-Liss, Inc.

引用

页码：200 / 201

页数：2

共 7 条

[1]

Ascher KW., 1920, KLIN MONATSBL AUGENH, V65, P86

[2] CONGENITAL DOUBLE LIP - REPORT OF 5 CASES AND A REVIEW OF THE LITERATURE [J].

BENMEIR, P ;

WEINBERG, A ;

NEUMAN, A ;

ELDAD, A ;

LUSTHAUS, S ;

ROTEM, M ;

WEXLER, MR .

ANNALS OF PLASTIC SURGERY, 1992, 28 (02) :180-182

[3]

FREIDHOFER H, 1991, REV HOSP CLIN FM SOO, V46, P126

[4]

GORLIN RJ, 2001, SYNDROME HEAD NECK

[5] DOUBLE LOWER LIP [J].

MAHLER, D ;

BARUCHIN, A .

ANNALS OF PLASTIC SURGERY, 1982, 8 (03) :248-249

[6]

Narang R, 1970, J Indian Dent Assoc, V42, P112

[7]

REDDY AK, 1998, PLAST RECONSTR SURG, V84, P420

← 1 →