Literature DB >> 16789632

Resistance to growth hormone releasing hormone and gonadotropins in Albright's hereditary osteodystrophy.

Giovanna Mantovani1, Anna Spada.   

Abstract

Heterozygous inactivating mutations in the Gs alpha gene cause Albright's hereditary osteo-dystrophy (AHO). Consistent with the observation that only maternally inherited mutations lead to resistance to hormone action (pseudohypoparathyroidism type Ia [PHP-Ia), recent studies have provided evidence for a predominant maternal origin of Gs alpha transcripts in endocrine organs, such as thyroid, gonad and pituitary. Accordingly, patients with PHP-Ia display variable degrees of resistance to parathyroid hormone (PTH), thyroid stimulating hormone (TSH), gonadotropins and growth hormone (GH) releasing hormone (GHRH). Although the incidence and the clinical and biochemical characteristics of PTH and TSH resistance have been widely investigated and described, the cause and significance of the reproductive dysfunction in AHO is still poorly understood. The clinical finding of alterations of GH secretion in these patients was described for the first time only 2 years ago. The present report briefly reviews the literature focusing on the actual knowledge about these last two subjects.

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Year:  2006        PMID: 16789632     DOI: 10.1515/jpem.2006.19.s2.663

Source DB:  PubMed          Journal:  J Pediatr Endocrinol Metab        ISSN: 0334-018X            Impact factor:   1.634


  10 in total

Review 1.  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

2.  Intraarticular heterotopic ossification as the initial manifestation in a child with pseudohypoparathyroidism 1a.

Authors:  Vijaya Sarathi; Abhishek Patil; Roshan Wade; Tushar R Bandgar; Nalini S Shah
Journal:  Indian J Pediatr       Date:  2011-01-13       Impact factor: 1.967

3.  Deletion of Gαq/11 or Gαs Proteins in Gonadotropes Differentially Affects Gonadotropin Production and Secretion in Mice.

Authors:  George A Stamatiades; Chirine Toufaily; Han Kyeol Kim; Xiang Zhou; Iain R Thompson; Rona S Carroll; Min Chen; Lee S Weinstein; Stefan Offermanns; Ulrich Boehm; Daniel J Bernard; Ursula B Kaiser
Journal:  Endocrinology       Date:  2022-02-01       Impact factor: 4.736

4.  The Association of Pseudohypoparathyroidism Type Ia with Chiari Malformation Type I: A Coincidence or a Common Link?

Authors:  Paria Kashani; Madan Roy; Linda Gillis; Olufemi Ajani; M Constantine Samaan
Journal:  Case Rep Med       Date:  2016-09-14

5.  Novel Mutation in PTHLH Related to Brachydactyly Type E2 Initially Confused with Unclassical Pseudopseudohypoparathyroidism.

Authors:  Jihong Bae; Hong Seok Choi; So Young Park; Do Eun Lee; Sihoon Lee
Journal:  Endocrinol Metab (Seoul)       Date:  2018-06

6.  Identification of a novel GNAS mutation in a case of pseudohypoparathyroidism type 1A with normocalcemia.

Authors:  Xiao-Dan Long; Jing Xiong; Zhao-Hui Mo; Chang-Sheng Dong; Ping Jin
Journal:  BMC Med Genet       Date:  2018-07-30       Impact factor: 2.103

7.  GNAS mutation is an unusual cause of primary adrenal insufficiency: a case report.

Authors:  Yajie Tong; Dongmei Yue; Ying Xin; Dan Zhang
Journal:  BMC Pediatr       Date:  2022-08-04       Impact factor: 2.567

8.  A patient with pseudohypoparathyroidism type 1A previously misdiagnosed as hereditary multiple exostosis: A case report.

Authors:  Jie Zhang; Ming Guan; Shiyong Zhao; Suling Wu; Lingwei Weng; Wenbin Sheng
Journal:  Exp Ther Med       Date:  2022-07-28       Impact factor: 2.751

9.  Plurihormone secreting pituitary macroadenoma masquerading as thyrotoxicosis: Clinical presentation and diagnostic challenges.

Authors:  Indira Maisnam; Deep Dutta; Rajesh Jain; Sujoy Ghosh; Satinath Mukhopadhyay; Subhankar Chowdhury
Journal:  Indian J Endocrinol Metab       Date:  2012-12

10.  Follow-up Findings in a Turkish Girl with Pseudohypoparathyroidism Type Ia Caused by a Novel Heterozygous Mutation in the GNAS Gene.

Authors:  Sezgin Şahin; Olaf Hiort; Susanne Thiele; Olcay Evliyaoğlu; Beyhan Tüysüz
Journal:  J Clin Res Pediatr Endocrinol       Date:  2016-07-18
  10 in total

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