Definitive evidence for an autosomal recessive form of hypohidrotic ectodermal dysplasia clinically indistinguishable from the more common X- linked disorder

F. Munoz, G. Lestringant, V. Sybert, M. Frydman, A. Alswaini, P. M. Frossard, R. Jorgenson, Jonathan (Jon) Zonana

Research output: Contribution to journalArticle

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Abstract

A crucial issue in genetic counseling is the recognition of nonallelic genetic heterogeneity. Hypohidrotic (anhidrotic) ectodermal dysplasia (HED), a genetic disorder characterized by defective development of hair, teeth, and eccrine sweat glands, is usually inherited as an X-linked recessive trait mapped to the X-linked ectodermal dysplasia locus, EDA, at Xq12-q13.1. The existence of an autosomal recessive form of the disorder had been proposed but subsequently had been challenged by the hypothesis that the phenotype of severely affected daughters born to unaffected mothers in these rare families may be due to marked skewing of X inactivation. Five families with possible autosomal recessive HED have been identified, on the basis of the presence of severely affected females and unaffected parents in single sibships and in highly consanguineous families with multiple affected family members. The disorder was excluded from the EDA locus by the lack of its cosegregation with polymorphic markers flanking the EDA locus in three of five families. No mutations of the EDA gene were detected by SSCP analysis in the two families not excluded by haplotype analysis. The appearance of affected males and females in autosomal recessive HED was clinically indistinguishable from that seen in males with X-linked HED. The findings of equally affected males and females in single sibships, as well as the presence of consanguinity, support an autosomal recessive mode of inheritance. The fact that phenotypically identical types of HED can be caused by mutations at both X-linked and autosomal loci is analogous to the situation in the mouse, where indistinguishable phenotypes are produced by mutations at both X-linked (Tabby) and autosomal loci (crinkled and downless).

Original languageEnglish (US)
Pages (from-to)94-100
Number of pages7
JournalAmerican Journal of Human Genetics
Volume61
Issue number1
StatePublished - Jul 1997

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Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
Ectodermal Dysplasia
Anhidrotic Ectodermal Dysplasia 1
Mutation
Eccrine Glands
Phenotype
Consanguinity
Single-Stranded Conformational Polymorphism
X Chromosome Inactivation
Sweat Glands
X-Linked Genes
Inborn Genetic Diseases
Genetic Heterogeneity
Genetic Counseling
Nuclear Family
Hair
Haplotypes
Tooth
Parents
Mothers

ASJC Scopus subject areas

  • Genetics

Cite this

Definitive evidence for an autosomal recessive form of hypohidrotic ectodermal dysplasia clinically indistinguishable from the more common X- linked disorder. / Munoz, F.; Lestringant, G.; Sybert, V.; Frydman, M.; Alswaini, A.; Frossard, P. M.; Jorgenson, R.; Zonana, Jonathan (Jon).

In: American Journal of Human Genetics, Vol. 61, No. 1, 07.1997, p. 94-100.

Research output: Contribution to journalArticle

Munoz, F. ; Lestringant, G. ; Sybert, V. ; Frydman, M. ; Alswaini, A. ; Frossard, P. M. ; Jorgenson, R. ; Zonana, Jonathan (Jon). / Definitive evidence for an autosomal recessive form of hypohidrotic ectodermal dysplasia clinically indistinguishable from the more common X- linked disorder. In: American Journal of Human Genetics. 1997 ; Vol. 61, No. 1. pp. 94-100.
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