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Article
| IMSEAR
| ID: sea-185422
ABSTRACT
Back ground: Holt-Oram is rare autosomal disorder, clinically characterised by congenital cardiac defects and morphological abnormalities of the upper limbs. Case characteristics:10 days old neonate born to first degree consangunious parents presented with upper limb anomaly and cardiac defects. Obseravations : Hypoplastic left thumb with ASD, VSD and PDAwas present. Message- Neonate with upper limb anomaly should be evaluated for congenital hear disease