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pubmed-article:3405592pubmed:abstractTextThe inheritance of Bardet-Biedl syndrome is thought to be autosomal recessive. Of the approximately 500 case reports in the literature, three patients were found to have sex chromosome aneuploidy. The authors describe two siblings with Bardet-Biedl syndrome, one of whom has a unique sex chromosome aneuploidy with mosaicism, including deletion of the short arm of the X chromosome (45,X/46,X,del(X)(p21)). The possible significance of sex chromosome aneuploidy and the Bardet-Biedl syndrome is discussed.lld:pubmed
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pubmed-article:3405592pubmed:articleTitleSex chromosome aneuploidy and Bardet-Biedl syndrome.lld:pubmed
pubmed-article:3405592pubmed:affiliationDivision of Ophthalmology, Case Western Reserve University, Cleveland, OH.lld:pubmed
pubmed-article:3405592pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:3405592pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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