Literature DB >> 14671404

Genetic basis for resistance to parathyroid hormone.

Michael A Levine1, Emily Germain-Lee, Suzanne Jan de Beur.   

Abstract

Pseudohypoparathyroidism (PHP) is associated with biochemical hypoparathyroidism (i.e. hypocalcemia and hyperphosphatemia) due to parathyroid hormone (PTH) resistance rather than to PTH deficiency. Patients with PHP type 1a have a generalized form of hormone resistance plus a constellation of developmental defects termed Albright hereditary osteodystrophy (AHO). Within PHP type 1a families some individuals will show AHO but have normal hormone responsiveness, a variant phenotype termed pseudo-PHP. By contrast, patients with PHP type 1b manifest only PTH resistance and lack features of AHO. These various forms of PHP are due to defects in the GNAS1 gene that lead to decreased expression or activity of the alpha-subunit of the stimulatory G protein (G(s)alpha). Tissue-specific genomic imprinting of GNAS1 accounts for the variable phenotypes of patients with GNAS1 defects. Copyright 2003 S. Karger AG, Basel

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Year:  2003        PMID: 14671404     DOI: 10.1159/000074508

Source DB:  PubMed          Journal:  Horm Res        ISSN: 0301-0163


  8 in total

1.  Clinical heterogeneity of familial pseudohypoparathyroidism.

Authors:  L Foppiani; P Del Monte; F Faravelli; L de Sanctis; A Marugo; D Bernasconi
Journal:  J Endocrinol Invest       Date:  2006-01       Impact factor: 4.256

2.  Bone mineral density in pseudohypoparathyroidism type 1a.

Authors:  Dominique N Long; Michael A Levine; Emily L Germain-Lee
Journal:  J Clin Endocrinol Metab       Date:  2010-07-07       Impact factor: 5.958

3.  Ossifications in Albright Hereditary Osteodystrophy: Role of Genotype, Inheritance, Sex, Age, Hormonal Status, and BMI.

Authors:  Parissa Salemi; Julie M Skalamera Olson; Lauren E Dickson; Emily L Germain-Lee
Journal:  J Clin Endocrinol Metab       Date:  2018-01-01       Impact factor: 5.958

4.  Polyglandular Autoimmune Syndrome Type III with Primary Hypoparathyroidism.

Authors:  Sang Jin Kim; Sang-Yoon Kim; Han-Byul Kim; Hyukwon Chang; Ho-Chan Cho
Journal:  Endocrinol Metab (Seoul)       Date:  2013-09-13

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

Review 6.  Management of pseudohypoparathyroidism.

Authors:  Emily L Germain-Lee
Journal:  Curr Opin Pediatr       Date:  2019-08       Impact factor: 2.856

7.  Parental Origin of Gsα Inactivation Differentially Affects Bone Remodeling in a Mouse Model of Albright Hereditary Osteodystrophy.

Authors:  Patrick McMullan; Peter Maye; Qingfen Yang; David W Rowe; Emily L Germain-Lee
Journal:  JBMR Plus       Date:  2021-11-16

8.  Bariatric surgery in an obese patient with Albright hereditary osteodystrophy: a case report.

Authors:  Chiara Ferrario; Giacomo Gastaldi; Luc Portmann; Vittorio Giusti
Journal:  J Med Case Rep       Date:  2013-04-24
  8 in total

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