Literature DB >> 23304807

GLI2 mutations as a cause of hypopituitarism.

Laurie E Cohen1.   

Abstract

The sonic hedgehog (Shh) signaling pathway is important in pituitary and craniofacial development. Gli2 is a transcription factor that mediates Shh signaling. Mutations in GLI2 have been found in association with holoprosencephaly (HPE) and HPE-like phenotype, with and without pituitary hormone deficiencies; as well as in patients with pituitary dysfunction with and without HPE craniofacial features. Polydactyly is a common associated finding.

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Year:  2012        PMID: 23304807

Source DB:  PubMed          Journal:  Pediatr Endocrinol Rev        ISSN: 1565-4753


  2 in total

Review 1.  Extracephalic manifestations of nonchromosomal, nonsyndromic holoprosencephaly.

Authors:  Ariel F Martinez; Paul S Kruszka; Maximilian Muenke
Journal:  Am J Med Genet C Semin Med Genet       Date:  2018-05-15       Impact factor: 3.908

2.  IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype.

Authors:  Isabelle Perrault; Jan Halbritter; Jonathan D Porath; Xavier Gérard; Daniela A Braun; Heon Yung Gee; Hanan M Fathy; Sophie Saunier; Valérie Cormier-Daire; Sophie Thomas; Tania Attié-Bitach; Nathalie Boddaert; Michael Taschner; Markus Schueler; Esben Lorentzen; Richard P Lifton; Jennifer A Lawson; Meriem Garfa-Traore; Edgar A Otto; Philippe Bastin; Catherine Caillaud; Josseline Kaplan; Jean-Michel Rozet; Friedhelm Hildebrandt
Journal:  J Med Genet       Date:  2015-08-14       Impact factor: 6.318

  2 in total

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