Niemann–Pick Disease Type C

Niemann-Pick disease type C (NPC) is a disabling, lysosomal-storage disorder that has been diagnosed prenatally, neonatally, during childhood, and even into adulthood.

Niemann-Pick disease type C, Orphanet Journal of Rare Diseases

Niemann-Pick disease types A and B (NORD): Video

Intrathecal 2-hydroxypropyl-β-cyclodextrin decreases neurological disease progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1–2 trial - The Lancet

Immune dysfunction in Niemann‐Pick disease type C - Platt - 2016 - Journal of Neurochemistry - Wiley Online Library

Mitochondrial dysfunction in fibroblasts derived from patients with Niemann-Pick type C disease - ScienceDirect

Niemann-Pick Type C « Niemann-Pick Children's Fund, Inc

Niemann-Pick disease type C. The diagram represents subtypes and onset

Niemann-Pick Disease Type C

Niemann–Pick disease - Wikipedia

Niemann Pick Disease Type C - Symptoms, Causes, Treatment

Niemann-Pick disease type C1 is a sphingosine storage disease that causes deregulation of lysosomal calcium