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

• Autores principales: Reema Garegrat (Autor), Suprabha K Patnaik (Autor), Nandini Malshe (Autor), Sandip P Bartakke (Autor), Vibha Bafna (Autor), Pradeep Suryawanshi (Autor)
• Formato: Libro
• Publicado: Wolters Kluwer Medknow Publications, 2022-01-01T00:00:00Z.
• Materias: article
• Acceso en línea: Connect to this object online.

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...