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X-linked disorders among patients with suspected genetic disorders attending the genetic clinic in Alexandria
Alexandria Journal of Pediatrics. 2006; 20 (1): 169-175
in En | IMEMR | ID: emr-75672
Responsible library: EMRO
ABSTRACT
A total of 1825 patients referred to the Genetics Clinic, Medical Research Institute, Alexandria University were assessed to determine the frequency of X-linked disorders. It was found that 3.0% [55/1825 cases; 52 males and 3 females] had X-linked disorders; 31.0% [17/55] had fragile X-syndrome 21.8% [12/55] had androgen insensitivity syndrome, 14.5% [8/55] had muscular dystrophy, 14.5% [8/55] had biochemical disorders and 18.2% [10/55] had X-linked syndromes. The frequency of consanguinity among parents of cases with X-linked disorders was 29.1%. Positive family history was detected in 29.1% of cases. These findings are crucial for geneticists and genetic counsellers in their evaluation, diagnosis, counseling and management of patients
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Index: IMEMR Main subject: Genetic Testing / Polymerase Chain Reaction / Consanguinity / Cytogenetic Analysis / Electroencephalography / Electrophoresis / Genetic Counseling Limits: Female / Humans / Male Language: En Journal: Alex. J. Pediatr. Year: 2006
Search on Google
Index: IMEMR Main subject: Genetic Testing / Polymerase Chain Reaction / Consanguinity / Cytogenetic Analysis / Electroencephalography / Electrophoresis / Genetic Counseling Limits: Female / Humans / Male Language: En Journal: Alex. J. Pediatr. Year: 2006