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.
CITATION STYLE
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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