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...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2017-09-01
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Series: | BMC Research Notes |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s13104-017-2803-6 |