Case report reveals Niemann-Pick type A and patent ductus arteriosus in an infant, indicating need for systemic evaluation.
Acid sphingomyelinase (ASM) deficiency leads to impaired lysosomal degradation of sphingomyelin and produces the clinical spectrum known as Niemann–Pick disease (types A and B). The infantile neurovisceral phenotype (type A) presents early in life with progressive neurologic impairment and multiorgan involvement. We report on a seven-month-old boy evaluated for recurrent respiratory illness who was incidentally found to have a small patent ductus arteriosus (PDA) on echocardiography. Physical examination revealed coarse facies, hepatosplenomegaly and developmental delay, while ophthalmologic assessment demonstrated bilateral cherry-red maculae. Molecular testing identified a homozygous nonsense variant in the SMPD1 gene, confirming Niemann–Pick disease type A. Association of this metabolic disorder with a structural cardiac lesion is unusual and highlights the importance of comprehensive systemic assessment in infants suspected of storage disorders.
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Kundu et al. (2026) studied this question.
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