Scarcity of mutations detected in families with X linked hypohidrotic ectodermal dysplasia

Diagnostic implications

Betsy Ferguson, N. S T Thomas, F. Munoz, D. Morgan, A. Clarke, Jonathan (Jon) Zonana

Research output: Contribution to journalArticle

33 Citations (Scopus)

Abstract

Indirect molecular diagnosis of X linked hypohidrotic ectodermal dysplasia (XLHED), a congenital disorder of hair, teeth, and eccrine sweat glands, has been possible by linkage analysis. Direct mutation detection would enable carrier detection in female relatives of sporadic cases, as well as help distinguish XLHED from the rarer, clinically indistinguishable, autosomal recessive disorder ARHED. Recently, a candidate gene for XLHED has been identified. Genomic DNA from 162 affected males and 21 females, who were either obligate carriers or had manifestations of the disorder, were screened by SSCP analysis. A subset of the patients had been previously screened for large genomic deletions and had limited screening of a single exon by SSCP analysis. The two known exons were amplified using flanking primers. Approximately 7% of patients, all males, had putative mutations identified within exon 1, but no variants were found within exon 2. Ten different putative mutations and four probable polymorphisms were identified. Both of the known exons were sequenced in 10 patients who had no detectable SSCP changes, but no additional mutations were found. No correlation between phenotype and genotype was evident between either affected subjects or subjects with or without detectable mutations. The results of the study indicate that only a small minority of affected males can be diagnosed by direct mutation analysis, and that the remainder of the patients are likely to have mutations in as yet unidentified exons of the EDA gene. Linkage analysis, in informative situations, therefore remains the only practical diagnostic option available.

Original languageEnglish (US)
Pages (from-to)112-115
Number of pages4
JournalJournal of Medical Genetics
Volume35
Issue number2
StatePublished - 1998

Fingerprint

Anhidrotic Ectodermal Dysplasia 1
Exons
Mutation
Single-Stranded Conformational Polymorphism
Eccrine Glands
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Sweat Glands
X-Linked Genes
Genetic Association Studies
Hair
Tooth
DNA

Keywords

  • Diagnosis
  • Hypohidrotic ectodermal dysplasia
  • Mutation

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Scarcity of mutations detected in families with X linked hypohidrotic ectodermal dysplasia : Diagnostic implications. / Ferguson, Betsy; Thomas, N. S T; Munoz, F.; Morgan, D.; Clarke, A.; Zonana, Jonathan (Jon).

In: Journal of Medical Genetics, Vol. 35, No. 2, 1998, p. 112-115.

Research output: Contribution to journalArticle

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