Exclusion of RNX as a major gene in congenital central Hypoventilation syndrome (CCHS, Ondine's curse)

被引:13
作者
Amiel, J
Pelet, A
Trang, H
de Pontual, L
Simonneau, M
Munnich, A
Gaultier, C
Lyonnet, S
机构
[1] Hop Necker Enfants Malad, Dept Genet, F-75743 Paris 15, France
[2] Hop Necker Enfants Malad, INSERM U393, F-75743 Paris, France
[3] Hop Robert Debre, Serv Physiol, F-75019 Paris, France
[4] Hop Robert Debre, INSERM E9935, F-75019 Paris, France
来源
AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 2003年 / 117A卷 / 01期
关键词
congenital central hypoventilation syndrome; Ondine's curse; Haddad syndrome; Hirschsprung disease; RNX gene;
D O I
10.1002/ajmg.a.10934
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Congenital central hypoventilation syndrome (CCHS) is a rare condition for which segregation analyses have suggested genetic factors. The respiratory phenotype of Rnx knock-out mice together with the Rnx expression at the brainstem level prompted us to consider the RNX gene as a candidate for CCHS in human. The screening of the RNX gene in a series of 25 patients with CCHS did not reveal any significant nucleotide variation. We therefore conclude that RNX is not a major gene for CCHS in human. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:18 / 20
页数:3
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