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Congenital dyserythropoietic anemia type IV with kruppel-like factor 1 E325K mutation in a preterm neonate: Case and literature review

Background: Clinical, pathologic, and genetic heterogeneity is a challenge in identifying and classifying congenital dyserythropoietic anemia (CDA). CDA type IV, the rarest CDA with only 11 reported cases, results from KLF1 gene mutation. Clinical Description: A male preterm neonate presented with j...

Ausführliche Beschreibung

Gespeichert in:
Hauptverfasser: Reema Garegrat, Suprabha K Patnaik, Nandini Malshe, Sandip P Bartakke, Vibha Bafna, Pradeep Suryawanshi
Format: Artigo
Sprache:Inglês
Veröffentlicht: Wolters Kluwer Medknow Publications 2022-01-01
Schriftenreihe:Indian Pediatrics Case Reports
Schlagworte:
congenital dyserythropoietic anemia
congenital dyserythropoietic anemia type iv
kruppel-like factor 1 mutation; neonate
Online-Zugang:http://www.ipcares.org/article.asp?issn=2772-5170;year=2022;volume=2;issue=2;spage=102;epage=106;aulast=Garegrat
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