TY  - JOUR 
TI  - Síndrome de Seckel, Dos Casos en una Familia Colombiana
PB  - Sociedad Chilena de Pediatría
PY  - 2010
issn 0370-4106
AB  - Seckel syndrome is an infrequent autosomic recessive genetic disorder. It is characterized by short stature, mental retardation and a typical facies. Nearly 10 families have been reported with two or more affected members.This paper reports two sisters, daughters of non-related parents. The mother presented bilateral fissurate lip. The main traits of this syndrome are highlighted through a literature review.

KW  - Enfermedades congénitas
KW  - Microcefalia
KW  - Enanismo
KW  - Labio fisurado
KW  - Síndrome
UR  - http://hdl.handle.net/10906/81247
ER  -