Literature DB >> 33552638

Pseudohypoparathyroidism with Ectopic Calcification and 22q11 Deletion Syndrome: A Rare Case.

Bruna Lixinski Diniz1, Andressa Barreto Glaeser1, Desirée Deconte1, Bruna Baierle Guaraná2, Rafael Fabiano Machado Rosa2, Paulo Ricardo Gazzola Zen2.   

Abstract

Ectopic calcification in soft tissue is associated with several disorders including pseudohypoparathyroidism (PHP), which is characterized by resistance or nonresponse to parathyroid hormone (PTH) function. Association between PHP and 22q11DS, also known as DiGeorge syndrome, is rare, especially in children. We describe a newborn girl diagnosed with 22q11DS, presenting ectopic calcifications in soft tissue and suspicion of PHP. PTH function showed values close to the upper limit of the reference value. Radiology showed bone callus in the right wrist. PHP can be a new clinical finding associated with 22q11DS. Parathyroid function investigation in individuals with 22q11DS, presenting bone dysmorphisms and/or calcium metabolism alterations, should be considered. Thieme. All rights reserved.

Entities:  

Keywords:  DiGeorge syndrome; ectopic calcification; pseudohypoparathyroidism

Year:  2020        PMID: 33552638      PMCID: PMC7853921          DOI: 10.1055/s-0040-1701640

Source DB:  PubMed          Journal:  J Pediatr Genet        ISSN: 2146-460X


  12 in total

Review 1.  Pseudohypoparathyroidism.

Authors:  Agnès Linglart; Michael A Levine; Harald Jüppner
Journal:  Endocrinol Metab Clin North Am       Date:  2018-10-12       Impact factor: 4.741

2.  Early manifestation of calcinosis cutis in pseudohypoparathyroidism type Ia associated with a novel mutation in the GNAS gene.

Authors:  Felix G Riepe; Wiebke Ahrens; Nils Krone; Regina Fölster-Holst; Jochen Brasch; Wolfgang G Sippell; Olaf Hiort; Carl-Joachim Partsch
Journal:  Eur J Endocrinol       Date:  2005-04       Impact factor: 6.664

3.  Hypothyroidism in patients with pseudohypoparathyroidism type Ia: clinical evidence of resistance to TSH and TRH.

Authors:  Anne-Sophie Balavoine; Miriam Ladsous; Fritz-Line Velayoudom; Virginie Vlaeminck; Catherine Cardot-Bauters; Michèle d'Herbomez; Jean-Louis Wemeau
Journal:  Eur J Endocrinol       Date:  2008-10       Impact factor: 6.664

4.  Prevalence of 22q11 microdeletion.

Authors:  S Tézenas Du Montcel; H Mendizabai; S Aymé; A Lévy; N Philip
Journal:  J Med Genet       Date:  1996-08       Impact factor: 6.318

Review 5.  Pseudohypoparathyroidism. New insights into an old disease.

Authors:  M Bastepe; H Jüppner
Journal:  Endocrinol Metab Clin North Am       Date:  2000-09       Impact factor: 4.741

6.  Body mass index differences in pseudohypoparathyroidism type 1a versus pseudopseudohypoparathyroidism may implicate paternal imprinting of Galpha(s) in the development of human obesity.

Authors:  Dominique N Long; Sarah McGuire; Michael A Levine; Lee S Weinstein; Emily L Germain-Lee
Journal:  J Clin Endocrinol Metab       Date:  2006-12-12       Impact factor: 5.958

7.  Progressive extreme heterotopic calcification.

Authors:  Margherita Silengo; Claudio Defilippi; Elga Belligni; Elisa Biamino; Elisabetta Flex; Alfredo Brusco; Giovanni Battista Ferrero; Marco Tartaglia; Raoul C Hennekam
Journal:  Am J Med Genet A       Date:  2013-05-17       Impact factor: 2.802

8.  A novel mutation causing pseudohypoparathyroidism 1A with congenital hypothyroidism and osteoma cutis.

Authors:  Tamar Lubell; Maria Garzon; Kwame Anyane Yeboa; Bina Shah
Journal:  J Clin Res Pediatr Endocrinol       Date:  2009-08-06

9.  A typical 22q11.2 deletion syndrome and pseudohypoparathyroidism: A CARE compliant case report.

Authors:  Xi-Juan Liu; Chen Yan; Jing-Yu Jia
Journal:  Medicine (Baltimore)       Date:  2019-06       Impact factor: 1.817

10.  Ectopic calcification as discernible manifestation in neonates with pseudohypoparathyroidism type 1a.

Authors:  Masanori Adachi; Koji Muroya; Yumi Asakura; Yoichi Kondoh; Jun Ishihara; Tomonobu Hasegawa
Journal:  Int J Endocrinol       Date:  2009       Impact factor: 3.257

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