Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12104/41445
Title: Familial iridogoniodysgenesis and skeletal anomalies: A probable new autosomal recessive disorder
Author: Rodriguez-Rojas, L.X.
Garcia-Cruz, D.
Mendoza-Topete, R.
Barba, L.B.
Barrios, M.T.
Patino-Garcia, B.
Lopez-Cardona, M.G.
Nuno-Arana, I.
Garcia-Ortiz, J.E.
Cantu, J.M.
Issue Date: 2004
Abstract: Three sibs with congenital glaucoma, skeletal anomalies, and peculiar facial appearance were studied. At birth, enlarged eyes and corneae were present in the proposita and her two brothers due to congenital glaucoma secondary to iridogoniodysgenesis (IGD). The purpose of this article is to describe the second familial case with IGD and skeletal anomalies as the family previously described by Garc� a-Cruz et al. in 1990, corroborating this new distinct dysmorphic syndrome with probable autosomal recessive inheritance. � Blackwell Munksgaard, 2004.
URI: http://www.scopus.com/inward/record.url?eid=2-s2.0-3242735059&partnerID=40&md5=99d7460424c9e2cd58f28fe6be5a7453
http://hdl.handle.net/20.500.12104/41445
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