Abstract |
DiGeorge syndrome is not really a rare disease. A microdeletion of chromosome 22q11.2 is found in most patients. Sharing the same genetic cause, a wide spectrum of clinical manifestations such as conotruncal anomaly face syndrome, Cayler cardiofacial syndrome, and velocardiofacial syndrome have been reported. Classic characteristics are cardiac defects, abnormal facial features, thymic hypoplasia, cleft palate, and hypocalcemia. We report a 6-year-old female child presenting with generalized seizure resulting from hypocalcemia. She had no cardiac defects and no hypocalcemia episode in neonatal stage, and had been said to be normal before by her parents until the diagnosis was made. This highlights the importance of extracardiac manifestations in the diagnosis of DiGeorge syndrome, and many affected patients may be underestimated with minor facial dysmorphism. As health practitioners, it is our duty to identify the victims undermined in the population, and start thorough investigations and the following rehabilitation as soon as possible. Multiplex ligation-dependent probe amplification is a rapid, reliable, and economical alternative for the diagnosis of 22q11.2 deletion.
|
Authors | Chih-Hsuan Fu, Cheung Leung, Chuan-Hong Kao, Shu-Jen Yeh |
Journal | Journal of the Formosan Medical Association = Taiwan yi zhi
(J Formos Med Assoc)
Vol. 114
Issue 8
Pg. 769-73
(Aug 2015)
ISSN: 0929-6646 [Print] Singapore |
PMID | 26254176
(Publication Type: Case Reports, Journal Article)
|
Copyright | Copyright © 2012. Published by Elsevier B.V. |
Topics |
- Brain
(diagnostic imaging, pathology)
- Child
- Chromosome Deletion
- Chromosomes, Human, Pair 22
- DiGeorge Syndrome
(diagnosis, genetics)
- Female
- Humans
- Multiplex Polymerase Chain Reaction
- Seizures
(etiology)
- Tomography, X-Ray Computed
|