Neonatal hemolytic anemia does not always indicate thalassemia: a case report

Abstract Background Congenital erythropoietic porphyria is a rare autosomal recessive disorder that affects heme-porphyrin synthesis. This disorder is due to the genetic defect of uroporphyrinogen III cosynthase. This defect results in the accumulation of high amounts of uroporphyrin I in all tissue...

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Bibliographic Details
Main Authors: Arwa A. Al-Harazi, Bilguis M. Al-Eryani, Butheinah A. Al-Sharafi
Format: Article
Language:English
Published: BMC 2017-09-01
Series:BMC Research Notes
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13104-017-2803-6