A case of partial trisomy 22 due to paternal 11;22 translocation, t(11;22)(q25;q13.1) / 대한산부인과학회잡지
Korean Journal of Obstetrics and Gynecology
;
: 1601-1605, 2002.
Artículo
en Coreano
| WPRIM
| ID: wpr-186413
ABSTRACT
Trisomy 22 is a frequent finding in spontaneous abortion. However, survival to term is tenuous. So far there have been about 85 cases of trisomy 22. Most of all cases, trisomy 22 was result of 31 meiotic segregation in the maternal 11;22 translocation carrier. These patients have a supernumerary, abnormal chromosome 22 [der(22)], in their chromosome constitution 47,XX(or XY),+der(22),t(11q;22q). Affected children have a distinct phenotype with multiple anomalies and severe mental retardation. We now report a viable case of 47,XX,+der(22)t(11;22)(q25;q13.1) resulting from 31 segregation in paternal translocation.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Fenotipo
/
Trisomía
/
Cromosomas Humanos Par 22
/
Aborto Espontáneo
/
Constitución y Estatutos
/
Discapacidad Intelectual
Límite:
Niño
/
Femenino
/
Humanos
/
Embarazo
Idioma:
Coreano
Revista:
Korean Journal of Obstetrics and Gynecology
Año:
2002
Tipo del documento:
Artículo
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