Niemann-Pick type A disease with new mutation: a case report

Fatemeh Aghamahdi1, Matineh Nirouei2, Shahram Savad3

  • 1Pediatric Endocrinologist, Department of Pediatrics, Alborz University of Medical Sciences, Karaj, Iran.

Summary

Niemann-Pick type A is a rare genetic disorder causing sphingomyelin buildup. This case study identifies a new mutation in the SMPD1 gene, offering insights into this severe childhood disease.

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