WAARDENBURG-I SYNDROME - A CLINICAL AND GENETIC-STUDY OF 2 LARGE BRAZILIAN KINDREDS, AND LITERATURE-REVIEW

被引：29

作者：

DASILVA, EO ^{[1
]}

机构：

[1] FED UNIV PERNAMBUCO,DEPT GEN BIOL,GENET LAB,RECIFE,PE,BRAZIL

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1991年 / 40卷 / 01期

关键词：

HETEROCHROMIA IRIDIS; HYPOPIGMENTATION; NEUROCRISTOPATHY; GENETIC HETEROGENEITY; AUTOSOMAL DOMINANT INHERITANCE;

D O I：

10.1002/ajmg.1320400113

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

Two large kindreds with Waardenburg I syndrome are described. The total number of affected individuals is 73. The major manifestations are telecanthus (the only constant anomaly in all cases), prominent nasal root, round or square tip of nose, hypoplastic alae, smooth philtrum, bushy eyebrows with synophrys, sensorineural deafness, heterochromia or hypoisochromia iridis, hypopigmented ocular fundus, white forelock, premature greying, and hypopigmented skin lesions. These and other aspects of the syndrome, associated findings, frequency, genetic heterogeneity, pathogenesis, animal models, and gene linkage and mapping are reviewed briefly.

引用

页码：65 / 74

页数：10

共 76 条

[1] WAARDENBURG AND HIRSCHSPRUNG SYNDROMES
AMBANI, LM
[J]. JOURNAL OF PEDIATRICS, 1983, 102 (05) : 802 - 802
[2] AMINIELIHOU S, 1970, J GENET HUM, V18, P307
[3] ANTUNES ERG, 1988, AN BRAS DERMATOL, V63, P75
[4] ARIAS S, 1975, HUMANGENETIK, V27, P145
[5] ARIAS S, 1971, Birth Defects Original Article Series, V7, P87
[6] BASILE R, 1965, J GENET HUM, V214, P87
[7] Boniface L, 1966, Ann Pediatr (Paris), V13, P788
[8] BRANSKI D, 1979, PEDIATRICS, V63, P803
[9] Calmettes L, 1968, Bull Mem Soc Fr Ophtalmol, V81, P144
[10] CARAKUSHANKSY G, 1975, REV ASSOC MED BRAS, V21, P159

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