Cytogenetic analysis of Down syndrome in Gujarat.
Indian Pediatr
;
2007 Oct; 44(10): 774-7
Artículo
en Inglés
| IMSEAR
| ID: sea-12769
ABSTRACT
During 1995 to 2006, 382 cases clinically suspected for Down syndrome were investigated for cytogenetic study. Free trisomy 21 constituted 84.8% of cases, translocation 8.9%, mosaic 3.9% and in 2.4% cases regular T21 was associated with structural or numerical changes. Translocation was parentally inherited in 26.5% cases and maternal transmission was twice as common as paternal. Males were more pronounced to be affected than females in all the groups. 91.6% of DS babies were born to younger mothers (20-35 yr) compared to 8.4% in elderly mothers (>35 yr).
Texto completo:
Disponible
Índice:
IMSEAR (Asia Sudoriental)
Asunto principal:
Femenino
/
Humanos
/
Masculino
/
Recién Nacido
/
Niño
/
Preescolar
/
Adolescente
/
Edad Materna
/
Síndrome de Down
/
Adulto
País/Región como asunto:
Asia
Idioma:
Inglés
Revista:
Indian Pediatr
Año:
2007
Tipo del documento:
Artículo
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