A Novel Mutation in a Child with Atypical Wiskott-Aldrich Syndrome Complicated by Cytomegalovirus Infection
Journal Title: Turkish Journal of Hematology - Year 2019, Vol 36, Issue 1
Abstract
.
Authors and Affiliations
Zühre Kaya, Cansu Muluk, Şule Haskoloğlu, Lale Ş. Tufan
Genotype-Phenotype Correlations of β-Thalassemia Mutations in an Azerbaijani Population
β-Thalassemia is the most common inherited disorder in Azerbaijan. The aim of our study was to reveal genotype-to-phenotype correlations of the most common β-thalassemia mutations in an Azerbaijani population. Patients w...
First Observation of Hemoglobin Jabalpur [Beta 3 (NA3) Leu>Pro] in the Turkish Population
First Observation of Hemoglobin San Diego, a High Oxygen Affinity Hemoglobin Variant, in Turkey
.
Aplastic anemia presenting as hemophagocytic lymphohistiocytosis
Two unusual cases of hemophagocytic lymphohistiocytosis (HLH) complicating aplastic anemia (AA) are described. Each patient had a history of preexisting acute hepatitis of unknown cause at the time of HLH diagnosis and i...
About Chediak-Higashi, Hemoglobin Lansing, and Hemoglobin Jabalpur