Novel COL4A1 mutations identified in infants with congenital hemolytic anemia in association with brain malformations
Hiromi Ogura1, Shouichi Ohga2, Takako Aoki1
1Department of Transfusion Medicine and Cell Processing, Tokyo Women's Medical University, Tokyo, Japan.
Human Genome Variation
|December 10, 2020
Abstract:
Genetic causes of undiagnosed hemolytic anemia in nineteen patients were analyzed by whole-exome sequencing, and novel COL4A1 variants were identified in four patients (21%). All patients were complicated with congenital malformations of the brain, such as porencephaly or schizencephaly. In these patients, hemolysis became less severe within 2 months after birth, and red cell transfusion was no longer required after 50 days, whereas chronic hemolysis continued.
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