Niemann-Pick disease - Breda Genetics srl Breda Genetics srl
Por um escritor misterioso
Last updated 14 junho 2024
The eponym Niemann-Pick disease (NPD) encompasses two distinct metabolic defects. The first includes NPD types A and B and is due to deficiency of the acid sphingomyelinase (ASM) enzyme. The second defect, namely NPD type C, is mainly due to accumulation of unesterified cholesterol and glycosphingolipids within the late endosome/lysosome of all cells.
Distinct Niemann-Pick Disease Type C Clinical, Cytological, and Biochemical Phenotype in an Adult Patient With 1 Mutated, Overexpressed NPC1 Allele - Julia Jecel, Klaus Harzer, Eduard Paschke, Stefanie Beck-Wödl, Peter Bauer, Milos
Genetics Screening and Testing - Breda Genetics srl
Breda Genetics srl - ITALY (@Breda_Genetics) / X
Breda Genetics srl - ITALY (@Breda_Genetics) / X
Niemann–Pick disease - Wikipedia
Three-years misdiagnosis of Niemann Pick disease type B with novel mutations in SMPD1 gene as Budd-Chiari syndrome, BMC Medical Genomics
Breda Genetics srl - ITALY (@Breda_Genetics) / X
Breda Genetics srl - ITALY (@Breda_Genetics) / X
Lysosomal and Mitochondrial Liaisons in Niemann-Pick Disease
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