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Biotinidase deficiency and juvenile myelomonocytic leukemia in a Turkish infant of consanguineous parents
Authors:Yetgin Sevgi  Aytac Selin  Kalkanoglu Serap  Coskun Turgay  Ortmann Christina  Kratz Christian  Niemeyer Charlotte
Affiliation: a Department of Pediatric Hematology, Hacettepe University, Ankara, Turkeyb Department of Pediatric Metabolism, Hacettepe University, Ankara, Turkeyc Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, University of Freiburg, Freiburg, Germany
Abstract:Here, a case is presented with two rare genetic disorders, biotinidase deficiency and juvenile myelomonocytic leukemia, in a Turkish infant. This case may serve as a reminder that the diagnosis of a genetic disorder does not exclude the possibility of a second congenital but acquired disease.
Keywords:biotinidase deficiency  juvenile myelomonocytic leukemia
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