Morphology of Niemann-Pick type A metabolic storage disorder

An Italian girl, of nonconsanguineous parents, had normal growth and development but at 1 year, hepatosplenomegaly was noted. An older sister was norm

Lysosomal Storage Diseases Diagram

IJMS, Free Full-Text

Niemann–Pick disease

Lysosomal storage diseases—the horizon expands

TPC2 rescues lysosomal storage in mucolipidosis type IV, Niemann–Pick type C1, and Batten disease

Finding pathogenic commonalities between Niemann-Pick type C and other lysosomal storage disorders: Opportunities for shared therapeutic interventions - ScienceDirect

Pathophysiology of neuropathic lysosomal storage disorders - Bellettato - 2010 - Journal of Inherited Metabolic Disease - Wiley Online Library

Gaucher disease with foamy transformed macrophages and erythrophagocytic activity - Machaczka - 2011 - Journal of Inherited Metabolic Disease - Wiley Online Library

A proposed model for the pathogenesis of Niemann-Pick disease type

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

Niemann–Pick Disease Type C: Induced Pluripotent Stem Cell–Derived Neuronal Cells for Modeling Neural Disease and Evaluating Drug Efficacy - Daozhan Yu, Manju Swaroop, Mengqiao Wang, Ulrich Baxa, Rongze Yang, Yiping Yan, Turhan