DNA Testing for Fragile X Syndrome in School for Emotionally Severely Handicapped Children in Korea
Journal of Genetic Medicine
; : 83-86, 1998.
Article
em En
| WPRIM
| ID: wpr-35563
Biblioteca responsável:
WPRO
ABSTRACT
Though Fragile X syndrome is one of the most common inherited causes of mental retardation, it is not much detected yet in Korean population. One of the reason may be that the syndrome is not well known to the special education teachers as well as to the clinicians in this country. Thus, molecular test was undertaken to screen out fragile X syndrome in 122 children of two Korean schools for emotionally severely handicapped children. The subjects were all boys, previously known as having pervasive developmental disorder with or without mental retardation. Southern blot analysis of peripheral blood showed the abnormally enlarged (CGG)n repeat sequence associated with fragile X syndrome in two children. This finding suggests that the DNA testing for fragile X syndrome is warranted for Korean high risk population and that more concern about this syndrome is needed for the professionals who work for mentally handicapped children. The issues involved in genetic counseling for fragile X syndrome are discussed.
Palavras-chave
Texto completo:
1
Índice:
WPRIM
Assunto principal:
DNA
/
Southern Blotting
/
Pessoas com Deficiência
/
Crianças com Deficiência
/
Pessoas com Deficiência Mental
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Educação Inclusiva
/
Síndrome do Cromossomo X Frágil
/
Aconselhamento Genético
/
Coreia (Geográfico)
/
Deficiência Intelectual
Limite:
Child
/
Humans
País/Região como assunto:
Asia
Idioma:
En
Revista:
Journal of Genetic Medicine
Ano de publicação:
1998
Tipo de documento:
Article