DiGeorge Syndrome Presenting as Hypocalcaemia-Induced Seizures in Adulthood
Introduction. DiGeorge syndrome is a developmental defect commonly caused by a microdeletion on the long arm of chromosome 22 or less frequently by a deletion of the short arm of chromosome 10. Case report. We report a case of a gentleman with mild dysmorphic features who presented with hypocalcaemi...
Saved in:
Main Authors: | Adrian Zammit, Deborah Grech Marguerat, Josephine Psaila, Alexander Attard |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2013-01-01
|
Series: | Case Reports in Medicine |
Online Access: | http://dx.doi.org/10.1155/2013/923129 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Type III Mixed Cryoglobulinemia and Antiphospholipid Syndrome in a Patient With Partial DiGeorge Syndrome
by: Alice D. Chang, et al.
Published: (2006-01-01) -
Cardiovascular Malformations in CHARGE Syndrome with DiGeorge Phenotype: Two Case Reports
by: Kazushi Yasuda, et al.
Published: (2016-01-01) -
A First Case Report of DiGeorge Syndrome from Ethiopia Highlights Challenges in Identifying and Treating Children with Primary T-Cell Deficiencies in Low Resource Settings
by: Tinsae Alemayehu, et al.
Published: (2020-01-01) -
Denosumab-Induced Severe Hypocalcaemia in Chronic Kidney Disease
by: Ryan Jalleh, et al.
Published: (2018-01-01) -
Ventricular Arrhythmia Precipitated by Severe Hypocalcaemia Secondary to Primary Hypoparathyroidism
by: S. Ashwin Reddy
Published: (2019-01-01)