Biotinidase deficiency and juvenile myelomonocytic leukemia in a Turkish infant of consanguineous parents

YETGİN S., Aytac Ş. S., Kalkanoglu S., COŞKUN T., Ortmann C., Kratz C., ...Daha Fazla

Pediatric Hematology and Oncology, cilt.24, sa.6, ss.453-455, 2007 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 24 Sayı: 6
  • Basım Tarihi: 2007
  • Doi Numarası: 10.1080/08880010701451293
  • Dergi Adı: Pediatric Hematology and Oncology
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.453-455
  • Hacettepe Üniversitesi Adresli: Evet

Özet

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. Copyright © Informa Healthcare USA, Inc.