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...

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Detalhes bibliográficos

Principais autores:	Reema Garegrat, Suprabha K Patnaik, Nandini Malshe, Sandip P Bartakke, Vibha Bafna, Pradeep Suryawanshi
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Wolters Kluwer Medknow Publications 2022-01-01
coleção:	Indian Pediatrics Case Reports
Assuntos:	congenital dyserythropoietic anemia congenital dyserythropoietic anemia type iv kruppel-like factor 1 mutation; neonate
Acesso em linha:	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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