Scinovex
article Open Access

Congenital dyserythropoietic anemia type I: Rare case report

International Journal of Research in Medical Science · 2019 · Vol. 1(1) · pp. 16–17

Abstract

Introduction: Congenital dyserythropoietic anemia type 1 is characterized by autosomal recessive inheritance and a macrocytic anemia with dyserythropoietic features such as megaloblastoid changes, multinuclearity, and internuclear chromatin bridges. Case report: Here, we reporting a case of Congenital dyserythropoietic anemia type 1(CDA 1) in 4 years old girl who presented with fever and abdominal pain. Conclusion: Our case highlights the fact that diagnosis of CDA 1 can be made with high reliability by careful examination of bone marrow aspirate and Biochemical study.

Erythrocyte Function and PathophysiologyBlood properties and coagulationCaveolin-1 and cellular processesMacrocytic anemiaAnemiaMedicineBone marrow examinationBone marrowGirlPediatricsPathologyInternal medicineBiology
Citations
0
FWCI
0.00
field-weighted impact
References
0
Percentile
23%
vs. same field & year
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.