نتایج جستجو برای: pick disease

تعداد نتایج: 1499420  

2009
P. Sharma R. Kar S. Dutta H.P. Pati R. Saxena

We present 2 cases of Niemann Pick disease, type B with secondary sea-blue histiocytosis. Strikingly, in both cases the Pick cells were positive for tartrate resistant acid phosphatase, a finding hitherto described only in Gaucher cells. This report highlights the importance of this finding as a potential cytochemical diagnostic pitfall in the diagnosis of Niemann Pick disease.

Journal: :Indian pediatrics 1994
M K Jain V P Gharpure

Journal: :Indian pediatrics 2012
K N Vykuntaraju Hemalatha Lokanatha Shivananda

Niemann-Pick group of diseases are rare lysosomal storage disorders. The clinical phenotype is variable. We report a child who first time presented with tremors of tongue and tremors of one side of the body. On examination child had hemiparesis and hepatosplenomegaly. Bone marrow examination shows storage cells suggestive of Niemann-Pick cells and enzyme assay confirmed the diagnosis.

Journal: :Cell reports 2013
Sovan Sarkar Bernadette Carroll Yosef Buganim Dorothea Maetzel Alex H M Ng John P Cassady Malkiel A Cohen Souvik Chakraborty Haoyi Wang Eric Spooner Hidde Ploegh Joerg Gsponer Viktor I Korolchuk Rudolf Jaenisch

Autophagy dysfunction has been implicated in misfolded protein accumulation and cellular toxicity in several diseases. Whether alterations in autophagy also contribute to the pathology of lipid-storage disorders is not clear. Here, we show defective autophagy in Niemann-Pick type C1 (NPC1) disease associated with cholesterol accumulation, where the maturation of autophagosomes is impaired becau...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2008
Rodney E Infante Michael L Wang Arun Radhakrishnan Hyock Joo Kwon Michael S Brown Joseph L Goldstein

Egress of lipoprotein-derived cholesterol from lysosomes requires two lysosomal proteins, polytopic membrane-bound Niemann-Pick C1 (NPC1) and soluble Niemann-Pick C2 (NPC2). The reason for this dual requirement is unknown. Previously, we showed that the soluble luminal N-terminal domain (NTD) of NPC1 (amino acids 25-264) binds cholesterol. This NTD is designated NPC1(NTD). We and others showed ...

2013
Peter Bauer David J. Balding Hans H. Klünemann David E. J. Linden Daniel S. Ory Mercè Pineda Josef Priller Frederic Sedel Audrey Muller Harbajan Chadha-Boreham Richard W. D. Welford Daniel S. Strasser Marc C. Patterson

Niemann-Pick disease type C (NP-C) is a rare, autosomal-recessive, progressive neurological disease caused by mutations in either the NPC1 gene (in 95% of cases) or the NPC2 gene. This observational, multicentre genetic screening study evaluated the frequency and phenotypes of NP-C in consecutive adult patients with neurological and psychiatric symptoms. Diagnostic testing for NP-C involved NPC...

Journal: :Molecular Genetics and Metabolism 2017

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