Clinical manifestations and molecular genetics of seven patients with Niemann–Pick type-C: a case series with a novel variant
NPC presents with diverse clinical findings across ages. Early hepatic symptoms in infants and neuropsychiatric issues in older patients warrant a high index of suspicion for NPC in such cases. A multidisciplinary approach is crucial for patient management, and further research is needed to clarify genotype-phenotype relationships in NPC.
Authors
- Engi̇n Köse (ORCID: https://orcid.org/0000-0001-7238-2894)
- Fatma Tuba Eminoğlu (ORCID: https://orcid.org/0000-0002-5880-1113)
- C J Kara
Institutions
- Ankara University (TR)
Publication Details
- Journal
- Journal of Pediatric Endocrinology and Metabolism
- Published
- 2025-01-10
- DOI
- https://doi.org/10.1515/jpem-2024-0530
- Primary Topic
- Lysosomal Storage Disorders Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00