Affiliation:
1. Universidad de Chile, Chile
Abstract
We report on a 14-year-old girl who presented a multiple congenital anomaly pattern: ablepharon, hypertelorism, telecanthus, macrostomia, helix agenesis of both ears, redundant thick skin and severe hirsutism, the 5th reported case of Barber-Say syndrome. Our patient had almost the same phenotype as that of the patient cited by Martínez Santana et al. (Am. J. Med. Genet. 47: 20-23, 1993) including the same until then undescribed dermatoglyphic pattern.
Subject
Genetics,Molecular Biology
Reference8 articles.
1. Macrostomia, ectropion, atrophic skin, hypertrichosis, and growth retardation;Barber N.;Syndrome Ident.,1982
2. Lid agenesis-macrostomia-psychomotor retardation-forehead hypertrichosis - a new syndrome? Am;Cesarino E.J.;J. Med. Genet.,1988
3. Macrostomia, ectropion, atrophic skin, hypertrichosis: another observation;David A.;Am. J. Med. Genet.,1991
4. Autosomal dominant inheritance of Barber-Say syndrome;Dinulos M.B.;Am. J. Med. Genet.,1999
5. Ablepharon macrostomia syndrome;Hornblass A.;Am. J. Ophthal.,1985
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