AUTOSOMAL RECESSIVE ECTODERMAL DYSPLASIA .1. AN UNDESCRIBED DYSPLASIA MALFORMATION SYNDROME

被引:31
作者
BUSTOS, T
SIMOSA, V
PINTOCISTERNAS, J
ABRAMOVITS, W
JOLAY, L
RODRIGUEZ, L
FERNANDEZ, L
RAMELA, M
机构
[1] INST VENEZOLANO INVEST CIENT,GENET HUMANA LAB,CARACAS 1010A,VENEZUELA
[2] HOSP DR AUGUSTIN R HERNANDEZ,NUEVA ESPARTA,VENEZUELA
[3] CTR MED DOCENTE LA TRINIDAD,CARACAS,VENEZUELA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1991年 / 41卷 / 04期
关键词
AUTOSOMAL RECESSIVE INHERITANCE; HYDROTIC ECTODERMAL DYSPLASIA; CLEFT LIP AND PALATE; PILI TORTI; SYNDACTYLY;
D O I
10.1002/ajmg.1320410403
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We describe 27 individuals of 7 families related to each other with high probability who showed manifestations of ectodermal dysplasia and other anomalies affecting females as severely as males with variable expressivity. All parents were normal. These families were detected in a relatively isolated and inbred population with very small neighbouring communities from a Carribbean Sea island, Margarita Island, in Northeastern Venezuela (Nueva Esparta State). The clinical picture common to all patients could not be classified within the heterogeneous group of known ectodermal dysplasias and the published cases do not resemble our patients. We believe that this condition constitutes a newly recognized autosomal recessive dysplasia/malformation syndrome of ectodermal dysplasia.
引用
收藏
页码:398 / 404
页数:7
相关论文
共 32 条
[1]  
ARIAS S, 1982, SKELETAL DYSPLASIAS, P487
[2]  
ARIAS S, 1981, 6TH INT C HUM GEN JE, P198
[3]  
BOWEN P, 1976, CLIN GENET, V9, P35
[4]  
BOWEN P, 1973, BIRTH DEFECTS ATLAS, P262
[5]  
Freire-Maia N, 1988, Birth Defects Orig Artic Ser, V24, P3
[6]  
FREIRE-MAIA N, 1973, Acta Biologica Paranaense, V2, P3
[7]  
FREIREMAIA N, 1987, REV BRAS GENET, V10, P403
[8]   ECTODERMAL DYSPLASIAS REVISITED [J].
FREIREMAIA, N .
ACTA GENETICAE MEDICAE ET GEMELLOLOGIAE, 1977, 26 (02) :121-131
[9]   ECTODERMAL DYSPLASIAS [J].
FREIREMAIA, N .
HUMAN HEREDITY, 1971, 21 (04) :309-+
[10]  
FREIREMAIA N, 1984, ECTODERMAL DYSPLASIS, P189