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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.
Journal of Medical Case Reports
|July 26, 2022
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.
Area of Science:
- Genetics
- Biochemistry
- Pediatrics
Background:
- Niemann-Pick type A (NP-A) is a severe, inherited lysosomal storage disorder.
- Caused by acid sphingomyelinase deficiency, leading to sphingomyelin accumulation and cellular damage.
- Characterized by hepatosplenomegaly, neurodegeneration, and failure to thrive, with a poor prognosis.
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