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

IF 0.4 Q4 PEDIATRICS Journal of pediatric genetics Pub Date : 2021-03-01 Epub Date: 2020-02-12 DOI:10.1055/s-0040-1701640
Bruna Lixinski Diniz, Andressa Barreto Glaeser, Desirée Deconte, Bruna Baierle Guaraná, Rafael Fabiano Machado Rosa, Paulo Ricardo Gazzola Zen
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引用次数: 2

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.

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假性甲状旁腺功能减退伴异位钙化和22q11缺失综合征:一例罕见病例。
软组织异位钙化与几种疾病有关,包括假性甲状旁腺功能低下(PHP),其特征是对甲状旁腺激素(PTH)功能有抵抗或无反应。PHP和22q11DS(也称为diggeorge综合征)之间的联系是罕见的,特别是在儿童中。我们描述了一个新生女孩诊断为22q11DS,表现为软组织异位钙化和怀疑PHP。PTH函数显示的值接近参考值的上限。放射学显示右手腕骨痂。PHP可能是与22q11DS相关的一个新的临床发现。应考虑对22q11DS患者进行甲状旁腺功能调查,这些患者出现骨畸形和/或钙代谢改变。
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期刊介绍: The Journal of Pediatric Genetics is an English multidisciplinary peer-reviewed international journal publishing articles on all aspects of genetics in childhood and of the genetics of experimental models. These topics include clinical genetics, molecular genetics, biochemical genetics, medical genetics, dysmorphology, teratology, genetic counselling, genetic engineering, formal genetics, neuropsychiatric genetics, behavioral genetics, community genetics, cytogenetics, hereditary or syndromic cancer genetics, genetic mapping, reproductive genetics, fetal pathology and prenatal diagnosis, multiple congenital anomaly syndromes, and molecular embryology of birth defects. Journal of Pediatric Genetics provides an in-depth update on new subjects and current comprehensive coverage of the latest techniques used in the diagnosis of childhood genetics. Journal of Pediatric Genetics encourages submissions from all authors throughout the world. The following articles will be considered for publication: editorials, original and review articles, short report, rapid communications, case reports, letters to the editor, and book reviews. The aim of the journal is to share and disseminate knowledge between all disciplines in the field of pediatric genetics. This journal is a publication of the World Pediatric Society: http://www.worldpediatricsociety.org/ The Journal of Pediatric Genetics is available in print and online. Articles published ahead of print are available via the eFirst service on the Thieme E-Journals platform.
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