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Case Reports
. 2021 Dec 10;35(4):535-541.
doi: 10.1515/jpem-2021-0052. Print 2022 Apr 26.

Niemann-Pick type C disease with a novel intronic mutation: three Turkish cases from the same family

Gonca Kılıç Yıldırım  1 , Coşkun Yarar  2 , Berna Şeker Yılmaz  3 , Serdar Ceylaner  4
Affiliations
Case Reports

Niemann-Pick type C disease with a novel intronic mutation: three Turkish cases from the same family

Gonca Kılıç Yıldırım et al. J Pediatr Endocrinol Metab. .

Abstract

Objectives: Niemann-Pick type C (NPC) disease is a rare progressive neurodegenerative condition that is characterized by the accumulation of cholesterol, glycosphingolipids, and sphingosine in lysosomes. Patients have various systemic and neurological findings depending on their age at onset. This disease is caused by the autosomal recessive transmission of mutations in the NPC1 and NPC2 genes; patients have mutations mainly in the NPC1 gene (95%) and the majority of them are point mutations located in the exonic regions.

Case presentation: Here, we presented three cousins with hepatosplenomegaly and progressive neurodegeneration who were diagnosed with visceral-neurodegenerative NPC disease. Their parents were relatives, and they had a history of sibling death with similar complaints. Bone marrow smear showed foamy cells in patient 1. Vertical supranuclear gaze palsy was not present in all cases. Sphingomyelinase (SM) activities were almost normal to exclude NPA or NPB. Filipin staining was performed in patient 2 and showed a massive accumulation of unesterified cholesterol The NPC1 gene analysis of the three patients showed a novel homozygous c.1553+5G>A intronic mutation. cDNA analysis was performed from the patient 3 and both parents. It was observed that exon 9 was completely skipped in the homozygous mutant baby. Both the normal and the exon 9-skipped transcripts have been detected in the parents.

Conclusions: When combined with the filipin staining and the patients' clinical outcomes, this mutation is likely to be deleterious. Moreover, cDNA sequencing supports the pathogenicity of this novel variant.

Keywords: NPC1gene; Niemann-Pick Type C (NPC); filipin test; neurodegeneration; novel mutation.

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