Literature DB >> 2047519

Pseudohypoparathyroidism: its phenotypic variability and associated disorders in a large family.

C M Faull1, R R Welbury, B Paul, P Kendall-Taylor.   

Abstract

Pseudohypoparathyroidism is a complex disorder of renal resistance to parathyroid hormone the mechanism of which is unclear. It is often associated with skeletal abnormalities and there may also be other hormonal defects. This is an extensive endocrinological investigation of five of six affected members in two generations of one family. The phenotypic variability of the syndrome is explored: four members had hypothyroidism; two had abnormal gonadal function; all five had abnormal prolactin response to TRH; one had abnormal hepatic response to glucagon infusion. All had normal hypothalamic-pituitary-adrenal axes, renal responsiveness to vasopressin and growth hormone responses to a variety of stimuli. Special note is made of oral pathology, and evidence of platelet aggregation abnormalities is presented which has not previously been described in the syndrome.

Entities:  

Mesh:

Year:  1991        PMID: 2047519

Source DB:  PubMed          Journal:  Q J Med        ISSN: 0033-5622


  14 in total

Review 1.  Clinical spectrum and pathogenesis of pseudohypoparathyroidism.

Authors:  M A Levine
Journal:  Rev Endocr Metab Disord       Date:  2000-11       Impact factor: 6.514

2.  A case of pseudohypoparathyroidism type la complicated with growth hormone deficiency: recovery of growth hormone secretion after vitamin D therapy.

Authors:  M Kaji; K Umeda; M Ashida; T Tajima
Journal:  Eur J Pediatr       Date:  2001-11       Impact factor: 3.183

3.  GH secretion in a cohort of children with pseudohypoparathyroidism type Ia.

Authors:  L de Sanctis; J Bellone; M Salerno; E Faleschini; M Caruso-Nicoletti; M Cicchetti; D Concolino; A Balsamo; F Buzi; L Ghizzoni; C de Sanctis
Journal:  J Endocrinol Invest       Date:  2007-02       Impact factor: 4.256

Review 4.  Pseudohypoparathyroidism and Gsα-cAMP-linked disorders: current view and open issues.

Authors:  Giovanna Mantovani; Anna Spada; Francesca Marta Elli
Journal:  Nat Rev Endocrinol       Date:  2016-04-22       Impact factor: 43.330

Review 5.  Imprinting in Albright's hereditary osteodystrophy.

Authors:  S J Davies; H E Hughes
Journal:  J Med Genet       Date:  1993-02       Impact factor: 6.318

Review 6.  Albright's hereditary osteodystrophy.

Authors:  L C Wilson; R C Trembath
Journal:  J Med Genet       Date:  1994-10       Impact factor: 6.318

Review 7.  Pseudohypoparathyroidism: one gene, several syndromes.

Authors:  O Tafaj; H Jüppner
Journal:  J Endocrinol Invest       Date:  2016-12-19       Impact factor: 4.256

8.  Pseudohypoparathyroidism in a mother and son: phenotypic variability and associated disorder.

Authors:  M Ray; J Goraya; S Basu; S Mitra; B Poddar; V Parmar
Journal:  Indian J Pediatr       Date:  2001-03       Impact factor: 1.967

Review 9.  The GNAS complex locus and human diseases associated with loss-of-function mutations or epimutations within this imprinted gene.

Authors:  Serap Turan; Murat Bastepe
Journal:  Horm Res Paediatr       Date:  2013-10-03       Impact factor: 2.852

10.  The GNAS Locus: Quintessential Complex Gene Encoding Gsalpha, XLalphas, and other Imprinted Transcripts.

Authors:  Murat Bastepe
Journal:  Curr Genomics       Date:  2007-09       Impact factor: 2.236

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.