Literature DB >> 9627600

Severe congenital hypopituitarism with low prolactin levels and age-dependent anterior pituitary hypoplasia: a clue to a PIT-1 mutation.

L Ward1, M Chavez, C Huot, P Lecocq, R Collu, J C Décarie, J A Martial, G Van Vliet.   

Abstract

A 20-month-old boy presented with severe congenital growth hormone, thyrotropin, and prolactin deficiencies resulting from a de novo mutation of the PIT-1 gene. This form of congenital hypopituitarism should be suspected if pituitary anatomy is normal, especially if prolactin levels are low and, in boys, if the external genitalia are normal. Pituitary atrophy appears to be an age-dependent phenomenon in this condition.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9627600     DOI: 10.1016/s0022-3476(98)70405-6

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  4 in total

Review 1.  Genetic aspects of central hypothyroidism.

Authors:  R Collu
Journal:  J Endocrinol Invest       Date:  2000-02       Impact factor: 4.256

Review 2.  Magnetic resonance imaging of the hypothalamus-pituitary unit in childrensuspected of hypopituitarism: who, how and when toinvestigate.

Authors:  M Maghnie; S Ghirardello; E Genovese
Journal:  J Endocrinol Invest       Date:  2004-05       Impact factor: 4.256

Review 3.  Genetic regulation of pituitary gland development in human and mouse.

Authors:  Daniel Kelberman; Karine Rizzoti; Robin Lovell-Badge; Iain C A F Robinson; Mehul T Dattani
Journal:  Endocr Rev       Date:  2009-10-16       Impact factor: 19.871

4.  Multiple pituitary hormone deficiency caused by pit-I mutation and the challenges of management in a developing country.

Authors:  O O Ayoola; F A Oladejo; M Dattani; P E Clayton
Journal:  Ann Ib Postgrad Med       Date:  2008-12
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.