Velocardiofacial syndrome case report: Is this a homogeneous genetic subtype of Schizophrenia?

South African Family Practice

 
 
Field Value
 
Title Velocardiofacial syndrome case report: Is this a homogeneous genetic subtype of Schizophrenia?
 
Creator Roos, J.L. Honey, E.M. Pretorius, H.W. Sobin, C. Karayiorgiou, M.
 
Subject — velocardiofacial syndrome; schizophrenia
Description In this case report of a 29 year old Afrikaner male, a diagnosis of velocardiofacial syndrome was made on clinical grounds. Later a FISH analysis test for 22q 11 microdeletion confirmed this clinical diagnosis. Specifically two independent studies have reported that 25-31% of patients with the 22q 11 microdeletion met diagnostic criteria for the schizophrenia or schizo-affective disorders, while the microdeletion occurs in the population at a rate of 0.025% it has been found in 2% of adult schizophrenia patients in the 6% of cases with childhood onset schizophrenia.
 
Publisher AOSIS
 
Contributor
Date 2003-05-31
 
Type info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion peer reviewed case studies —
Format application/pdf
Identifier 10.4102/safp.v45i2.1984
 
Source South African Family Practice; Vol 45, No 2 (2003); 4 2078-6204 2078-6190
 
Language eng
 
Relation
The following web links (URLs) may trigger a file download or direct you to an alternative webpage to gain access to a publication file format of the published article:

https://safpj.co.za/index.php/safpj/article/view/1984/2532
 
Coverage — — —
Rights https://creativecommons.org/licenses/by/4.0
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