Abstract
This is the case of a male newborn with a diagnosis of Patau syndrome; genetic cause was an uncommon variant, a reciprocal translocation between chromosomes 10 and 13. Clinical images of the patient as well as karyotype findings are presented.
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APA
Peláez-Cantero, M. J., Delicado-Calderón, I., & Sánchez-Torres, L. (2020). Patau syndrome by reciprocal translocation between chromosomes 10 and 13. Revista Mexicana de Pediatria, 87(6), 244–246. https://doi.org/10.35366/97689
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