Literature DB >> 19307682

Hypocalcaemia as presenting symptom of velocardiofacial syndrome.

E I van Vliet1, B M van Ouwerkerk.   

Abstract

Hypocalcaemia due to hypoparathyroidism is a rare finding in adults. The coexistence of cardiac abnormalities may be suggestive of a hereditary syndrome. We describe a case of velocardiofacial syndrome in a woman without a family history of this disorder. The hypocalcaemia was treated with calcium and vitamin D supplementation.

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Year:  2009        PMID: 19307682

Source DB:  PubMed          Journal:  Neth J Med        ISSN: 0300-2977            Impact factor:   1.422


  2 in total

1.  22q11.2 microdeletion in two adolescent patients who presented with convulsion.

Authors:  Murat Özkale; İlknur Erol
Journal:  Turk Pediatri Ars       Date:  2014-03-01

2.  An Adult Case of Chromosome 22q11.2 Deletion Syndrome Associated with a High-positioned Right Aortic Arch.

Authors:  Yoichi Hoshino; Moriya Machida; Shun-Ichi Shimano; Teizo Taya
Journal:  Intern Med       Date:  2017-04-01       Impact factor: 1.271

  2 in total

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