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...
Gorde:
| Egile Nagusiak: | , , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
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Wolters Kluwer Medknow Publications
2022-01-01
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| Saila: | Indian Pediatrics Case Reports |
| Gaiak: | |
| Sarrera elektronikoa: | 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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