Severe clinical course in a patient with congenital amegakaryocytic thrombocytopenia due to a missense mutation of the c-MPL gene C-MPL genindeki yanlış anlamlı mutasyona bağlı konjenital amegakaryositik trombositopenili bir hastada ağır klinik seyir


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Ok Bozkaya İ., Yaralı N. , Işık P., Saç R. Ü. , Tavil B., Tunç B.

Turkish Journal of Hematology, vol.32, no.2, pp.172-174, 2015 (Journal Indexed in SCI Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 32 Issue: 2
  • Publication Date: 2015
  • Doi Number: 10.4274/tjh.2013.0191
  • Title of Journal : Turkish Journal of Hematology
  • Page Numbers: pp.172-174
  • Keywords: Amino acid change, C-MPL, C-MPL Tryp154Arg, Congenital amegakaryocytic thrombocytopenia, Homozygous missense mutation, Thrombopoietin

Abstract

© 2015, Turkish Society of Hematology. All rights reserved.Congenital amegakaryocytic thrombocytopenia (CAMT) generally begins at birth with severe thrombocytopenia and progresses to pancytopenia. It is caused by mutations in the thrombopoietin receptor gene, the myeloproliferative leukemia virus oncogene (c-MPL). The association between CAMT and c-MPL mutation type has been reported in the literature. Patients with CAMT have been categorized according to their clinical symptoms caused by different mutations. Missense mutations of c-MPL have been classified as type II and these patients have delayed onset of bone marrow failure compared to type I patients. Here we present a girl with severe clinical course of CAMT II having a missense mutation in exon 4 of the c-MPL gene who was admitted to our hospital with intracranial hemorrhage during the newborn period.