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Genet Couns ; 16(1): 101-5, 2005.
Article in English | MEDLINE | ID: mdl-15844787

ABSTRACT

We describe a newborn with multiple congenital anomalies consistent with an oro-facio-digital syndrome (OFDS). These are a group of inherited syndromes that have in common anomalies of the tongue (bifid or lobulated tongue with hamartomas), the face (median cleft lip) and the digits (brachydactyly, polydactyly, clinodactyly and/or syndactyly). OFDS has been classified into 11 types. The case described in this paper had manifestations overlapping with OFDS II (Mohr) and OFDS IV (Mohr-Majewski) and OFDS VI (Varadi). We propose that the present patient has a new variation of the OFDS due to the co-existence of the very atypical combination of polydactyly, cerebellar hypoplasia, hypothalamic hamartoma and classical facial findings of OFDS.


Subject(s)
Brain Diseases/complications , Brain Diseases/genetics , Cerebellum/abnormalities , Face/abnormalities , Genetic Variation/genetics , Hamartoma/complications , Hamartoma/genetics , Hypothalamus , Orofaciodigital Syndromes/complications , Orofaciodigital Syndromes/genetics , Polydactyly/complications , Polydactyly/genetics , Brain Diseases/pathology , Foot Deformities, Congenital/complications , Foot Deformities, Congenital/diagnostic imaging , Hamartoma/pathology , Hand Deformities, Congenital/complications , Hand Deformities, Congenital/diagnostic imaging , Humans , Hypothalamus/pathology , Infant, Newborn , Magnetic Resonance Imaging , Male , Orofaciodigital Syndromes/pathology , Polydactyly/diagnosis , Tomography, X-Ray Computed
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