Chromosome 22q11.2 Deletion Syndrome Presenting as Adult Onset Hypoparathyroidism: Clues to Diagnosis from Dysmorphic Facial Features
Author:
Affiliation:
1. Department of Medicine, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok 10400, Thailand
Abstract
Publisher
Hindawi Limited
Subject
Endocrinology, Diabetes and Metabolism
Link
http://downloads.hindawi.com/journals/crie/2013/802793.pdf
Reference22 articles.
1. Hypoparathyroidism in the adult: Epidemiology, diagnosis, pathophysiology, target-organ involvement, treatment, and challenges for future research
2. Hypoparathyroidism
3. A Case of Chromosome 22q11 Deletion Syndrome Diagnosed in a 32-Year-Old Man with Hypoparathyroidism
4. Delayed-Onset Hypoparathyroidism in an Adolescent with Chromosome 22Q11 Deletion Syndrome
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2. An Endocrinological Perspective on 22q11.2 Deletion Syndrome: A Single-center Experience;Journal of Clinical Research in Pediatric Endocrinology;2023-08-23
3. Hypoparathyroidism and late-onset hypogonadism in an adult male with familial 22q11.2 deletion syndrome: a case report with 3-year follow-up and review of the literature;BMC Endocrine Disorders;2022-11-12
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