SciELO - Scientific Electronic Library Online

 
vol.3 issue1 author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

  • Have no cited articlesCited by SciELO

Related links

  • Have no similar articlesSimilars in SciELO

Share


Memorias del Instituto de Investigaciones en Ciencias de la Salud

On-line version ISSN 1812-9528

Abstract

HERREROS, MB; ATOBE, O  and  RODRIGUEZ, S. Prenatal diagnosis of ectrodactyly in two siblings. Mem. Inst. Investig. Cienc. Salud [online]. 2005, vol.3, n.1, pp.65-67. ISSN 1812-9528.

Ectrodactyly is a rare congenital malformation characterized by absence of digits and has a wide variety of expression. This anomaly can be sporadic or associated with various genetic and non-genetic syndromes such as the autosomal dominant Ectrodactyly and the Ectrodactyly and Ectodermal Dysplasia, Cleft Palate Syndrome (EEC). In this report, we present the cases of two brothers with a prenatal diagnosis of ectrodactyly by ultrasound in the second trimester of both pregnancies. The first pregnancy ended in the stillbirth of a male fetus with ectrodactyly of both hands and feet and stenosis of the umbilical cord. The second pregnancy resulted in the delivery of a boy with left hand agenesis and right hand and feet ectrodactyly. We highlight the importance of routine and thorough examination of fetal hands and feet during the second trimester ultrasound to make a better and more frequent diagnosis of hand and foot malformations.

Keywords : Eectrodactylyb; Prenatal diagnosis; Ultrasound.

        · abstract in Spanish     · text in Spanish     · Spanish ( pdf )

 

Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License