NAGER ACROFACIAL DYSOSTOSIS - MALE-TO-MALE TRANSMISSION IN 2 FAMILIES

被引:31
作者
AYLSWORTH, AS
LIN, AE
FRIEDMAN, PA
机构
[1] UNIV N CAROLINA,SCH MED,BRAIN & DEV RES CTR,CHAPEL HILL,NC 27514
[2] W PENN HOSP,DEPT MED GENET,PITTSBURGH,PA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1991年 / 41卷 / 01期
关键词
MANDIBULOFACIAL DYSOSTOSIS; LIMB ANOMALIES; HIRSCHSPRUNG DISEASE; NEURAL CREST; GENETICS; AUTOSOMAL DOMINANT;
D O I
10.1002/ajmg.1320410121
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We describe 2 unrelated families with male-to-male transmission of Nager syndrome. All 5 affected individuals have moderate expression of the phenotype. One affected boy also has Hirschsprung disease. Although Nager acrofacial dysostosis usually occurs sporadically, both recessive and dominant inheritance have been suggested on the basis of reported familial cases. The 2 families described here with father-to-son transmission strongly support the hypothesis that some cases of Nager acrofacial dysostosis occur in individuals who are heterozygous for dominantly expressed, autosomal mutations.
引用
收藏
页码:83 / 88
页数:6
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