Literature DB >> 29668551

Fetal-onset Congenital Dyserythropoietic Anemia Type 1 due to a Novel Mutation With Severe Iron Overload and Severe Cholestatic Liver Disease.

Hui-Lin Chin1,2, Le Ye Lee1,2, Pei Lin Koh1,2.   

Abstract

We report a rare case of severe congenital dyserythropoietic anemia type 1 with fetal onset. Our patient presented with fetal hydrops from 19 weeks of gestation, requiring multiple intrauterine transfusions. At birth, she had severe hemolytic anemia with severe jaundice, and was subsequently transfusion dependent. She eventually developed severe iron overload and fulminant liver failure before her demise at 5 months of age. Genetic testing revealed a novel mutation in CDAN1.

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Year:  2019        PMID: 29668551     DOI: 10.1097/MPH.0000000000001151

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  1 in total

1.  [Whole exome sequencing analysis of compound heterozygous variants of CDAN1 gene in a Chinese family with non-immune hydrops fetalis].

Authors:  Y Wang; Q Li; X Sun; S Li; J He; M Zhang; L Huang; W He
Journal:  Nan Fang Yi Ke Da Xue Xue Bao       Date:  2021-12-20
  1 in total

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