Barber-Say syndrome: further delineation of the clinical spectrum

Author:

Cortés Fanny M.1,Troncoso Ledia A.1,Alliende Angélica R.1,Curotto Bianca L.1

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.

Publisher

FapUNIFESP (SciELO)

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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1. Barber Say Syndrome (A new case report);Indian Dermatology Online Journal;2019

2. Barber-Say syndrome and Ablepharon-Macrostomia syndrome: An overview;American Journal of Medical Genetics Part A;2016-05-19

3. Recurrent Mutations in the Basic Domain of TWIST2 Cause Ablepharon Macrostomia and Barber-Say Syndromes;The American Journal of Human Genetics;2015-07

4. Diseases of Periocular Hair;Survey of Ophthalmology;2011-09

5. Oral and dental abnormalities in Barber-Say syndrome;American Journal of Medical Genetics Part A;2010-09-09

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