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PMID: 3873926 Published · ppublish fre English Abstract Journal Article

[Congenital adrenal hyperplasia (21-OH) in France. Population genetics].

L'hyperplasie congénitale des surrénales (21-OH) en France. Génétique des populations.

Archives francaises de pediatrie ·Vol. 42 ·No. 3 ·1985-03-00 ·Pages 175-9

Bois E, Mornet E, Chompret A, Feingold J, Hochez J, Goulet V

Abstract

Incidence of congenital adrenal hyperplasia due to 21 hydroxylase deficiency was studied in France. Five hundred and twenty six patients born during the period 1963-1979 were found. Assuming complete ascertainment in females, the incidence of the disease is 0.43 X 10(-4) or 1: 23,044. The frequency of the carriers is 0.013 (1/76). The birth places of patients show an unequal geographic distribution. The mean inbreeding coefficient is 270 X 10(-5), a figure higher than the mean coefficient of France. The frequency of marriages between first cousins is slightly raised, 0.3%.

MeSH Terms
Adrenal Hyperplasia, Congenital/diagnosis,epidemiology,genetics Child Child, Preschool Consanguinity Female France Genetics, Population Humans Infant Infant, Newborn Male
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Bois E
Mornet E
Chompret A
Feingold J
Hochez J
Goulet V
Article Info
Journal
Archives francaises de pediatrie
Abbr.
Arch Fr Pediatr
ISSN
0003-9764
Published
1985-03-00
Pages
175-9
Language
fre
Region
France
NLM ID
0372421
Subset
IM
External Links
PubMed source
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