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Updated: Sep 30, 2026

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
Intermediate-Phenotype ABCA3 Deficiency Caused by Compound Heterozygous Variants Presenting as Persistent Respiratory
Ammir Abuzahra1, Mohamad Abu Mayalah2, Mahmoud Abdelrazzaq Abu Mayaleh3,4
1College of Medicine, Hebron University Hebron Palestine.
Abstract:
ABCA3 deficiency should be suspected in term infants with persistent respiratory distress from birth. This case highlights how early whole-exome sequencing established the diagnosis after extensive investigations, identified an intermediate phenotype caused by compound heterozygous variants, and guided targeted multidisciplinary management.
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