BIOTINIDASE DEFICIENCY AND JUVENILE MYELOMONOCYTIC LEUKEMIA IN A TURKISH INFANT OF CONSANGUINEOUS PARENTS

Sevgi Yetgin Department of Pediatric Hematology, Hacettepe University, Ankara, Turkey

Selin Aytac Department of Pediatric Hematology, Hacettepe University, Ankara, Turkey

Serap Kalkanoglu Department of Pediatric Metabolism, Hacettepe University, Ankara, Turkey

Turgay Coskun Department of Pediatric Metabolism, Hacettepe University, Ankara, Turkey

Christina Ortmann Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, University of Freiburg, Freiburg, Germany

Christian Kratz Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, University of Freiburg, Freiburg, Germany

Charlotte Niemeyer Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, University of Freiburg, Freiburg, Germany

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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.

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BIOTINIDASE DEFICIENCY AND JUVENILE MYELOMONOCYTIC LEUKEMIA IN A TURKISH INFANT OF CONSANGUINEOUS PARENTS

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BIOTINIDASE DEFICIENCY AND JUVENILE MYELOMONOCYTIC LEUKEMIA IN A TURKISH INFANT OF CONSANGUINEOUS PARENTS

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