Literature DB >> 88082

Interpretation of isolated agenesis of the pituitary.

C Roux, R Dupuis, C Horvath, A Giroud.   

Abstract

Cholesterol synthesis inhibitors administered to rats caused more or less complete forms of the holoprosencephalic syndrome, consisting of severe abnormalities of the brain, sense organs and pituitary. The absence of the pituitary was also observed in fetuses without externally visible cephalic abnormalities. These observations suggest that the isolated absence of the pituitary is the lesser form of the holoprosencephalic syndrome. This interpretation is also valid for cases of isolated absence of the pituitary observed in humans.

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Year:  1979        PMID: 88082     DOI: 10.1002/tera.1420190107

Source DB:  PubMed          Journal:  Teratology        ISSN: 0040-3709


  2 in total

Review 1.  The Smith-Lemli-Opitz syndrome.

Authors:  R I Kelley; R C Hennekam
Journal:  J Med Genet       Date:  2000-05       Impact factor: 6.318

2.  Abnormal cholesterol biosynthesis in the Smith-Lemli-Opitz and the lethal acrodysgenital syndromes.

Authors:  V Cormier-Daire; C Wolf; A Munnich; M Le Merrer; A Nivelon; D Bonneau; H Journel; F Fellmann; F Chevy; C Roux
Journal:  Eur J Pediatr       Date:  1996-08       Impact factor: 3.183

  2 in total

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