Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency

Irène Netchine, Marie Laure Sobrier, Heiko Krude, Dirk Schnabel, Mohamed Maghnie, Elisabeth Marcos, Bénédicte Duriez, Valère Cacheux, Arpard V. Moers, Michel Goossens, Annette Grüters, Serge Amselem

Research output: Contribution to journalArticlepeer-review


Combined pituitary hormone deficiency (CPHD) has been linked with rare abnormalities in genes encoding transcription factors necessary for pituitary development. We have isolated LHX3, a gene involved in a new syndrome, using a candidate-gene approach developed on the basis of documented pituitary abnormalities of a recessive lethal mutation in mice generated by targeted disruption of Lhx3 (ref. 2). LHX3, encoding a member of the LIM class of homeodomain proteins, consists of at least six exons located at 9q34. We identified a homozygous LHX3 defect in patients of two unrelated consanguineous families displaying a complete deficit in all but one (adrenocorticotropin) anterior pituitary hormone and a rigid cervical spine leading to limited head rotation. Two of these patients also displayed a severe pituitary hypoplasia, whereas one patient presented secondarily with an enlarged anterior pituitary. These LHX3 mutations consist of a missense mutation (Y116C) in the LIM2 domain at a phylogenetically conserved residue and an intragenic deletion predicting a severely truncated protein lacking the entire homeodomain. These data are consistent with function of LHX3 in the proper development of all anterior pituitary cell types, except corticotropes, and extrapituitary structures.

Original languageEnglish
Pages (from-to)182-186
Number of pages5
JournalNature Genetics
Issue number2
Publication statusPublished - Jun 2000

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics


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