Van der Woude syndrome with sensorineural hearing loss, large craniofacial sinuses, dental pulp stones, and minor limb anomalies: Report of a four-generation Thai family

被引:17
作者
Kantaputra, PN [1 ]
Sumitsawan, Y
Schutte, BC
Tochareontanaphol, C
机构
[1] Chiang Mai Univ, Fac Dent, Sch Dent, Dept Pediat Dent, Chiang Mai 50200, Thailand
[2] Chiang Mai Univ, Fac Med, Dept Otolaryngol, Chiang Mai 50000, Thailand
[3] Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA
[4] Chromosome Ctr, Bangkok, Thailand
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 2002年 / 108卷 / 04期
关键词
dental anomaly; Van der Woude syndrome; brachymesophalangy; lip pit; pulp stone; large craniofacial sinuses; sensorineural hearing loss;
D O I
10.1002/ajmg.10276
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A four-generation Thai family affected with Van der Woude syndrome is reported. The disorder appeared to be originally inherited from a person who was half Thai and half Pakistani. The lip lesions found in this family were varied and did not appear to be related to other phenotypes. There were some clinical manifestations possibly specific for the condition in this family. They included sensorineural hearing loss, prominent frontal bone, large frontal/sphenoidal/ maxillary sinuses with increased mastoid air cells, long tooth roots, dental pulp stones, ankyloglossia, brachydactyly of hands, brachyphalangy, and hyperphalangy of toes, and single flexion crease of the fifth fingers. Fluorescence in situ hybridization analysis revealed no visible deletion at a 1q32-41 region. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:275 / 280
页数:6
相关论文
共 21 条
[1]  
BACIAN M, 1987, AM J MED GENET, V26, P437
[2]  
BURDICK AB, 1985, J CRAN GENET DEV BIO, V5, P181
[3]  
BURDICK AB, 1987, J CRAN GENET DEV BIO, V7, P413
[4]  
CALNAN J, 1952, BRIT J PLAST SURG, V5, P197
[5]  
CERVENKA J, 1967, AM J HUM GENET, V19, P416
[6]  
FRANCKE U, 1972, AM J HUM GENET, V24, P189
[7]  
Houdayer C, 2000, AM J MED GENET, V91, P161, DOI 10.1002/(SICI)1096-8628(20000313)91:2<161::AID-AJMG18>3.0.CO
[8]  
2-Q
[9]   THE VANDERWOUDE SYNDROME IN A LARGE KINDRED - VARIABILITY, PENETRANCE, GENETIC RISKS [J].
JANKU, P ;
ROBINOW, M ;
KELLY, T ;
BRALLEY, R ;
BAYNES, A ;
EDGERTON, MT .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1980, 5 (02) :117-123
[10]  
LEE MM, 1999, J MED GENET, V36, P888