SciELO - Scientific Electronic Library Online

 
vol.63 número4Tratamiento con fenestración: Reporte de un caso y revisiónAscaridiasis biliar en un paciente pediátrico. Reporte de caso índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados

Revista

Articulo

Indicadores

Links relacionados

  • No hay articulos similaresSimilares en SciELO

Compartir


Gen

versión impresa ISSN 0016-3503versión On-line ISSN 2477-975X

Resumen

SAUD, Anibal; ARTIS, Maria Teresa; CORDOBA, Keila  y  GUZMAN, Jojana. Herencia dominante de malformación anorrectal. Estudio en una familia . Gen [online]. 2009, vol.63, n.4, pp.292-295. ISSN 0016-3503.

The Malformations anorectal (MAR) are a group of congenital malformations characterized by the lack of union between the anal pit and duct anorectal. Affects men often slightly greater than in the women, and are presented in one of every 4000 to 5000 newborn. The estimated risk of a couple of having another child with a sea is about 1 %. Described in some cases by a recessive autosomal inheritance type but the recurrence in the brotherhood is generally low. We present a of newborn male with antenatal diagnosis of congenital megacolon vs. MAR physical examination is evidenced not permeable anus and is backed with invertograma with high MAR, finding which colostomy it´s why colostomy derivation itÊs mode, and at a second surgical time diagnoses intestinal malrotation. It´s made It is interesting to present it since three direct members of a family group have a history of congenital malformation of the tract gastrointestinal with clinical variety, being novel to stand out the hereditary transmission of this rare condition.

Palabras clave : anorectal; megacolon malformation.

        · resumen en Español     · texto en Español

 

Creative Commons License Todo el contenido de esta revista, excepto dónde está identificado, está bajo una Licencia Creative Commons