Mild to Severe Anemia of Undiagnosed Etiology Diagnosed by Genetic Study

We report a case of a child with beta thalassemia major, whose mother is a carrier of beta thalassemia and father is having hereditary persistence of fetal hemoglobin. Gene study revealed compound heterozygous for codon 8/9+G and IVS-1-5 G>C point mutation. Another four cases of anemia not respon...

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Veröffentlicht in:	Journal of Nepal Paediatric Society 2016-12, Vol.36 (2), p.213-215
Hauptverfasser:	Bose, Kalliol, Siddique, Md Abu Bakkar, Ghorai, Sudipta, Kundu, Chanchal, Saha, Sudip
Format:	Artikel
Sprache:	eng
Online-Zugang:	Volltext
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