Literature DB >> 21265963

22q11.2 deletion presenting with severe hypocalcaemia, seizure and basal ganglia calcification in an adult man.

Z Cao1, R Yu, K Dun, J Burke, N Caplin, T Greenaway.   

Abstract

We report a 40-year-old man who was found to have profound hypocalcaemia and hypoparathyroidism when investigated for multiple, generalized, tonic/clonic seizures and a chest infection. Computed tomography scan of the brain revealed extensive symmetric bilateral calcification within the cerebellum, thalamus and basal ganglia. Molecular cytogenetic testing by fluorescent in situ hybridization using the commercial Vysis LSI DiGeorge/VCFS dual colour probe set showed a deletion of 22q11.2. The extraordinary feature of this case is the adult presentation of hypocalcaemia, hypoparathyroidism and basal ganglia calcification due to 22q11.2 deletion.
© 2011 The Authors. Internal Medicine Journal © 2011 Royal Australasian College of Physicians.

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Year:  2011        PMID: 21265963     DOI: 10.1111/j.1445-5994.2010.02374.x

Source DB:  PubMed          Journal:  Intern Med J        ISSN: 1444-0903            Impact factor:   2.048


  5 in total

1.  Idiopathic Hypoparathyroidism (IHP) Presenting as "Schizophrenia:" A Case Report.

Authors:  Hanna Lu
Journal:  Noro Psikiyatr Ars       Date:  2014-12-01       Impact factor: 1.339

2.  Recurrent convulsions, hypocalcemia, and hypoparathyroidism related to delayed diagnosis of 22q11.2 deletion syndrome in a middle-aged man.

Authors:  Tomoya Okazaki; Toru Hifumi; Tomohiro Ibata; Arisa Manabe; Hideyuki Hamaya; Takuo Yoshimoto; Hitomi Imachi; Koji Murao; Kenya Kawakita; Yasuhiro Kuroda
Journal:  Acute Med Surg       Date:  2016-05-02

3.  Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects.

Authors:  Emilia Cirillo; Giuliana Giardino; Vera Gallo; Pamela Puliafito; Chiara Azzari; Rosa Bacchetta; Fabio Cardinale; Maria Pia Cicalese; Rita Consolini; Silvana Martino; Baldassarre Martire; Cristina Molinatto; Alessandro Plebani; Gioacchino Scarano; Annarosa Soresina; Caterina Cancrini; Paolo Rossi; Maria Cristina Digilio; Claudio Pignata
Journal:  BMC Med Genet       Date:  2014-01-02       Impact factor: 2.103

4.  Neuroanatomical phenotypes in a mouse model of the 22q11.2 microdeletion.

Authors:  J Ellegood; S Markx; J P Lerch; P E Steadman; C Genç; F Provenzano; S A Kushner; R M Henkelman; M Karayiorgou; J A Gogos
Journal:  Mol Psychiatry       Date:  2013-09-03       Impact factor: 15.992

5.  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

  5 in total

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