Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindred.

Details

Serval ID
serval:BIB_326857B462AC
Type
Article: article from journal or magazin.
Collection
Publications
Title
Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindred.
Journal
Journal of endocrinological investigation
Author(s)
Nogueira C.R., Leite C.C., Chedid E.P., Liberman B., Pimentel-Filho F.R., Kopp P., Medeiros-Neto G.A.
ISSN
0391-4097 (Print)
ISSN-L
0391-4097
Publication state
Published
Issued date
06/1998
Peer-reviewed
Oui
Volume
21
Number
6
Pages
386-391
Language
english
Notes
Publication types: Case Reports ; Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Abstract
Familial hypopituitarism represents a clinically and genetically heterogeneous disorder. In a subset of these families, defects in Pit-I, a transcription factor essential for proper pituitary development have been identified as underlying molecular cause. These patients present extreme short stature, GH, PRL and TSH deficiency but intact ACTH, LH and FSH secretion. The pituitary is usually hypoplastic. In this report we describe a consanguineous family (the parents are first cousins) with thirteen siblings. Of the ten living siblings, four (two males and two females) have panhypopituitarism with severe growth failure. They had evidence of growth hormone, prolactin and gonadotropin deficiencies and developed central hypothyroidism late in life. ACTH secretion was normal. Bone age was retarded and dual-photon bone densitometry indicated severe osteoporosis. Combined provocative tests for pituitary hormones indicated blunted responses for GH, LH, FSH and a modest rise in serum PRL and TSH. A clonidine-test failed to induce pituitary GH response. A corticotropin-releasing factor (CRF) provocative test was conducted after 6 months without the use of prednisone with a normal ACTH response after CRF in the affected sibling. Plasma IGF-I and IGF-BP3 were below normal levels. Serum E2 (females) and serum testosterone (males) levels were very low. MRI evaluation of the pituitary indicated pituitary aplasia in all subjects. The phenotype described in this kindred is different from families reported with Pit-1 mutations. However, it resembles previously published kindreds with similar clinical and biochemical findings. The relative preservation of ACTH suggests a genetic defect early in pituitary gland development.
Keywords
Adolescent, Adrenocorticotropic Hormone/metabolism, Adult, Brazil, Consanguinity, Female, Follicle Stimulating Hormone/deficiency, Growth Disorders/etiology, Human Growth Hormone/deficiency, Humans, Hypopituitarism/genetics, Luteinizing Hormone/deficiency, Male, Pedigree, Pituitary Hormones/deficiency, Prolactin/deficiency, Thyrotropin/deficiency
Pubmed
Web of science
Create date
30/12/2020 15:36
Last modification date
31/12/2020 6:26
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