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dc.contributor.authorStavrou, Stavros S.
dc.contributor.authorZhu, Yuan Shan
dc.contributor.authorCai, LiQun
dc.contributor.authorKatz, Melissa D.
dc.contributor.authorHerrera, Cecilia
dc.contributor.authorDefilló Ricart, Mariano
dc.contributor.authorImperato McGinley, J.
dc.date.accessioned2018-11-28T18:37:47Z
dc.date.available2018-11-28T18:37:47Z
dc.date.issued1998
dc.identifier.citationStavrou SS, Zhu YS, Cai L, Katz MD, Herrera C, Defilló Ricart M, et al. A novel mutation of the human luteinizing hormone receptor in 46XY and 46XX sisters. JCE & M. 1998 ; 83(6) : 2091-2098.en
dc.identifier.issn0021972X
dc.identifier.urihttps://academic.oup.com/jcem/article/83/6/2091/2865544?searchresult=1
dc.description.abstractWe repor t a novel homozygous mutation of the LH receptor (LHR) gene in three siblings: two 46XY and one 46XX. The 46XY siblings presented with female external genitalia, primary amenorrhea, and lack of breast development. Hormonal evaluation revealed a markedly elevated LH level with a low testosterone level, which failed to increase after human CG stimulation. Enzymatic deficiencies of testosterone biosynthesis were eliminated as possible etiologies. Histologic analysis of the inguinal gonads in a 46XY sibling revealed no Leydig cells; Sertoli cells, spermatogonia, and primary spermatocytes were seen. The 46XX sibling had female external genitalia, normal breast development, and primary amenorrhea. Hormonal analyses showed markedly elevated LH levels and low plasma 17β-estradiol levels. Genetic analysis of the LHR revealed a homozygous missense mutation at exon 11 of the LHR gene. Guanine was replaced by adenine (GAA→AAA), resulting in a substitution of lysine for glutamic acid (glu) at amino acid position 354 of the receptor. This mutation is located in the extracellular domain adjacent to the first transmembrane helix of the LHR. Glutamic acid at position 354 of the LHR has been highly conserved throughout evolution. Functional analysis of the LHR mutation, using an in vitro mutagenesis-transfection assay, demonstrated complete loss of function, indicated by the lack of cAMP production after human CG stimulation in transfected human embryonic kidney 293 cells. Screening of family members demonstrated heterozygosity for the mutation, indicating autosomal recessive inheritance. Delineation of the specific genetic defect in this family confirms recent reports that a single mutation in the LHR gene causes male pseudohermaphroditism in 46XY subjects and primary amenorrhea in 46XX subjects. More importantly, it also defines a new region of the LHR molecule that is critical for biologic activity.en
dc.language.isoenen
dc.publisherJournal of Clinical Endocrinology and Metabolismen
dc.relation.ispartofseries83 (6)
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectTrastornos del desarrollo sexuales_ES
dc.subjectTrastorno del desarrollo sexual 46 XYes_ES
dc.subjectTrastorno del desarrollo sexual 46 XXes_ES
dc.subjectGenética humanaes_ES
dc.subjectMutaciónes_ES
dc.subjectHormonases_ES
dc.subjectEndocrinologíaes_ES
dc.subjectEstadísticas y datos numéricoses_ES
dc.titleA novel mutation of the human luteinizing hormone receptor in 46XY and 46XX sisters.en
dc.typeArticleen


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivatives 4.0 Internacional