Phenotypic heterogeneity in Woodhouse-Sakati syndrome: Two new families with a mutation in the C2orf37 gene

Tawfeg Ben-Omran, Rehab Ali, Mariam Almureikhi, Seham Alameer, Muna Al-Saffar, Christopher A. Walsh, Jillian M. Felie, Ahmad Teebi

Research output: Contribution to journalArticlepeer-review

24 Citations (Scopus)

Abstract

Hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome [also known as Woodhouse-Sakati syndrome (WSS)] is a rare autosomal recessive neuroendocrine and ectodermal disorder. The syndrome was first described by Woodhouse and Sakati in 1983, and 47 patients from 23 families have been reported so far. We report on an additional seven patients (four males and three females) from two highly consanguineous Arab families from Qatar, presenting with a milder phenotype of WSS. These patients show the spectrum of clinical features previously found in WSS, but lack evidence of diabetes mellitus and extrapyramidal symptoms. These two new families further illustrate the natural course and the interfamilial phenotypic variability of WSS that may lead to challenges in making the diagnosis. In addition, our study suggests that WSS may not be as infrequent in the Arab world as previously thought.

Original languageEnglish
Pages (from-to)2647-2653
Number of pages7
JournalAmerican Journal of Medical Genetics, Part A
Volume155
Issue number11
DOIs
Publication statusPublished - Nov 2011
Externally publishedYes

Keywords

  • Alopecia
  • Arab
  • Autosomal recessive
  • Deafness
  • Diabetes mellitus
  • Hypogonadism
  • Learning disabilities
  • Qatar
  • Woodhouse-Sakati syndrome

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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