Literature DB >> 12756381

Parathyroid function and growth in 22q11.2 deletion syndrome.

Raja Brauner1, Agnes Le Harivel de Gonneville, Catherine Kindermans, Jérone Le Bidois, Marguerite Prieur, Stanislaus Lyonnet, Jean-Claude Souberbielle.   

Abstract

OBJECTIVE: To determine the frequency and expression of hypoparathyroidism and the factors of short stature in 22q11.2 deletion syndrome to optimize clinical care. STUDY
DESIGN: Cross-sectional study of 39 patients 9.7 +/- 0.8 (2.5-20) years of age.
RESULTS: The congenital abnormalities were cardiac defects in 33 of 39, thymus hypoplasia in 15 of 18 evaluated, and craniofacial dysmorphy in all; 15 patients (39%) had had one or more seizures. Before evaluation, 12 patients were hypocalcemic, with (n = 4) or without clinical manifestations, diagnosed before 1 month in 10 cases, at 3 months or 12 years in two others. At evaluation, 9 patients were hypocalcemic, 5 of 9 had been hypocalcemic, and 8 others had parathyroid hormone (PTH) concentrations low for their ionized calcium. One had high PTH without hypocalcemia and 2 were hypercalcemic. The values were below -2 SD at birth for weight and/or height in 26% of cases and at evaluation for height and body mass index in 23% and for insulin-like growth factor-I in 37%.
CONCLUSIONS: Parathyroid function was abnormal in 27 of 39 (69%) patients. This was not diagnosed in the majority. Short stature was probably due to intrauterine growth restriction, underweight, and growth hormone deficiency, as suggested by low insulin-like growth factor I.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12756381     DOI: 10.1067/mpd.2003.156

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  11 in total

1.  Clinical features of 78 adults with 22q11 Deletion Syndrome.

Authors:  Anne S Bassett; Eva W C Chow; Janice Husted; Rosanna Weksberg; Oana Caluseriu; Gary D Webb; Michael A Gatzoulis
Journal:  Am J Med Genet A       Date:  2005-11-01       Impact factor: 2.802

2.  Influence of chromosome 22q11.2 microdeletion on postoperative calcium level after cardiac-correction surgery.

Authors:  Li Shen; Haitao Gu; Dongjing Wang; Chi Yang; Zhengfeng Xu; Hua Jing; Yongzhong Jiang; Yibing Ding; Huacheng Hou; Zhijuan Ge; Shilin Chen; Xuming Mo; Long Yi
Journal:  Pediatr Cardiol       Date:  2011-06-16       Impact factor: 1.655

3.  Vitamin D deficiency, behavioral atypicality, anxiety and depression in children with chromosome 22q11.2 deletion syndrome.

Authors:  L Kelley; A F P Sanders; E A Beaton
Journal:  J Dev Orig Health Dis       Date:  2016-12       Impact factor: 2.401

4.  Bone density assessment in a cohort of pediatric patients affected by 22q11DS.

Authors:  A Ficcadenti; F Zallocco; R Neri; L Giovannini; G Tirabassi; G Balercia
Journal:  J Endocrinol Invest       Date:  2015-04-28       Impact factor: 4.256

5.  Dynamic and structural properties of the skeleton in hypoparathyroidism.

Authors:  Mishaela R Rubin; David W Dempster; Hua Zhou; Elizabeth Shane; Thomas Nickolas; James Sliney; Shonni J Silverberg; John P Bilezikian
Journal:  J Bone Miner Res       Date:  2008-12       Impact factor: 6.741

6.  Molecular screening for 22Q11.2 deletion syndrome in patients with congenital heart disease.

Authors:  Janaína Huber; Vivian Catarino Peres; Alexandre Luz de Castro; Tiago Jeronimo dos Santos; Lauro da Fontoura Beltrão; Angélica Cerveira de Baumont; Silvia Liliana Cossio; Tiago Pires Dalberto; Mariluce Riegel; Andrés Delgado Cañedo; Beatriz D'Agord Schaan; Lucia Campos Pellanda
Journal:  Pediatr Cardiol       Date:  2014-06-01       Impact factor: 1.655

Review 7.  Practical guidelines for managing adults with 22q11.2 deletion syndrome.

Authors:  Wai Lun Alan Fung; Nancy J Butcher; Gregory Costain; Danielle M Andrade; Erik Boot; Eva W C Chow; Brian Chung; Cheryl Cytrynbaum; Hanna Faghfoury; Leona Fishman; Sixto García-Miñaúr; Susan George; Anthony E Lang; Gabriela Repetto; Andrea Shugar; Candice Silversides; Ann Swillen; Therese van Amelsvoort; Donna M McDonald-McGinn; Anne S Bassett
Journal:  Genet Med       Date:  2015-01-08       Impact factor: 8.822

8.  Clinical manifestations of Deletion 22q11.2 syndrome (DiGeorge/Velo-Cardio-Facial syndrome).

Authors:  Mc Digilio; B Marino; R Capolino; B Dallapiccola
Journal:  Images Paediatr Cardiol       Date:  2005-04

9.  Endocrine and Growth Disorders in Taiwanese Children With 22q11.2 Deletion Syndrome.

Authors:  Han-Yi Lin; Wen-Yu Tsai; Yi-Ching Tung; Shih-Yao Liu; Ni-Chung Lee; Yin-Hsiu Chien; Wuh-Liang Hwu; Cheng-Ting Lee
Journal:  Front Endocrinol (Lausanne)       Date:  2022-03-31       Impact factor: 5.555

10.  Chromosome 22q11.2 deletion syndrome presenting as adult onset hypoparathyroidism: clues to diagnosis from dysmorphic facial features.

Authors:  Sira Korpaisarn; Objoon Trachoo; Chutintorn Sriphrapradang
Journal:  Case Rep Endocrinol       Date:  2013-04-30
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.