Another case of preaxial polydactyly and white forelock in branchio-oculo-facial syndrome

被引：4
作者：
McGaughran, J [1 ]
机构：
[1] No Reg Genet Serv, Auckland, New Zealand
来源：
CLINICAL DYSMORPHOLOGY | 2001年 / 10卷 / 01期
关键词：
branchio-oculo-facial syndrome; polydactyly; white forelock;
D O I：
10.1097/00019605-200101000-00015
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
A 1-year-old male with branchio-oculo-facial syndrome together with preaxial polydatyly and a white forelock at birth is described. This is only the second case where preaxial polydactyly has been described in branchio-oculo-facial syndrome. In both cases a diagnosis of Waardenburg syndrome had been considered. Clin Dysmorphol 10: 67-68 (C) 2001 Lippincott Williams & Wilkins.
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收藏
页码：67 / 68
页数：2
相关论文
共 4 条
  • [1] NEW AUTOSOMAL DOMINANT BRANCHIOOCULOFACIAL SYNDROME
    FUJIMOTO, A
    LIPSON, M
    LACRO, RV
    SHINNO, NW
    BOELTER, WD
    JONES, KL
    WILSON, MG
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 27 (04): : 943 - 951
  • [2] HING AV, 1992, CLIN GENET, V41, P74
  • [3] FURTHER DELINEATION OF THE BRANCHIOOCULOFACIAL SYNDROME
    LIN, AE
    GORLIN, RJ
    LURIE, IW
    BRUNNER, HG
    VANDERBURGT, I
    NAUMCHIK, IV
    RUMYANTSEVA, NV
    STENGELRUTKOWSKI, S
    ROSENBAUM, K
    MEINECKE, P
    MULLER, D
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 56 (01): : 42 - 59
  • [4] Megarbane A, 1998, CLIN DYSMORPHOL, V7, P221
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