Barber-Say syndrome: Further delineation of the clinical spectrum

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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 Martinet Santana et al. including the same until then undescribed dermatoglyphic pattern.

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Cortes, F. M., Troncoso, L. A., Alliende, A. R., & Curotto, B. L. (2000). Barber-Say syndrome: Further delineation of the clinical spectrum. Genetics and Molecular Biology, 23(2), 265–267. https://doi.org/10.1590/S1415-47572000000200003

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