Literature DB >> 2120445

Very low levels of high density lipoprotein cholesterol in four sibs of a family with non-neuropathic Niemann-Pick disease and sea-blue histiocytosis.

M B Viana1, R Giugliani, V H Leite, M L Barth, C Lekhwani, C M Slade, A Fensom.   

Abstract

Very low serum levels of high density lipoprotein cholesterol ranging from 8.6 to 13.9 mg/dl were detected in four out of 12 sibs of a Brazilian kindred with the non-neuropathic form of Niemann-Pick disease. Hepatosplenomegaly, interstitial infiltration of the lungs, absence of neurological signs, sea-blue histiocytes in the bone marrow and liver, and high values for serum acid phosphatase (18 to 32 U/l) were common to all affected children. Leucocyte acid sphingomyelinase activity ranged from 3.6 to 6.5% of mean control values, and fibroblast activity from 9 to 13% of mean controls. The parents had low-normal levels. The relationship between these findings is unclear and deserves further investigation.

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Year:  1990        PMID: 2120445      PMCID: PMC1017198          DOI: 10.1136/jmg.27.8.499

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  22 in total

1.  A new form of Niemann-Pick disease characterised by temperature-labile sphingomyelinase.

Authors:  E L Schneider; P G Pentchev; S R Hibbert; A Sawitsky; R O Brady
Journal:  J Med Genet       Date:  1978-10       Impact factor: 6.318

2.  Nine cases of sphingomyelin lipidosis, a new variant in Spanish-American Children. Juvenile variant of Niemann-Pick Disease with foamy and sea-blue histiocytes.

Authors:  D A Wenger; G Barth; J H Githens
Journal:  Am J Dis Child       Date:  1977-09

3.  Studies in lipid histochemistry. XII. Histochemical detection of sphingomyelin.

Authors:  M Elleder; Z Lojda
Journal:  Histochemie       Date:  1973-12-31

4.  Letter: Sea-blue histiocytes in thrombocytopenic purpura.

Authors:  P Chandra; F Rosner; A Sawitsky
Journal:  Ann Intern Med       Date:  1973-12       Impact factor: 25.391

5.  Pathogenesis of one variant of sea-blue histiocytosis.

Authors:  D W Golde; E L Schneider; D F Bainton; P G Pentchev; R O Brady; C J Epstein; M J Cline
Journal:  Lab Invest       Date:  1975-10       Impact factor: 5.662

6.  Biochemical, genetic and ultrastructural study of a family with the sea-blue histiocyte syndrome/chronic non-neuronopathic Niemann-Pick disease.

Authors:  K Fried; S Beer; H I Krespin; H Leiba; M Djaldetti; D Zitman; C Klibansky
Journal:  Eur J Clin Invest       Date:  1978-08       Impact factor: 4.686

7.  Lecithin-cholesterol acyltransferase and the lipoprotein abnormalities of parenchymal liver disease.

Authors:  R C Day; D S Harry; J S Owen; A Y Foo; N McIntyre
Journal:  Clin Sci (Lond)       Date:  1979-01       Impact factor: 6.124

8.  Sea blue histiocytosis in a patient with chronic non-neuropathic Niemann-Pick disease.

Authors:  N Dewhurst; G T Besley; N D Finlayson; A C Parker
Journal:  J Clin Pathol       Date:  1979-11       Impact factor: 3.411

9.  The sea-blue histiocyte syndrome with hepatic porphyria and infectious mononucleosis.

Authors:  M L Ghosh
Journal:  J Clin Pathol       Date:  1972-11       Impact factor: 3.411

10.  Adult Niemann-Pick disease: its relationship to the syndrome of the sea-blue histiocyte.

Authors:  R G Long; B D Lake; J E Pettit; P J Scheuer; S Sherlock
Journal:  Am J Med       Date:  1977-04       Impact factor: 4.965

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  13 in total

Review 1.  Monogenic dyslipidemias: window on determinants of plasma lipoprotein metabolism.

Authors:  R A Hegele
Journal:  Am J Hum Genet       Date:  2001-10-26       Impact factor: 11.025

2.  Complementation studies in Niemann-Pick disease type C indicate the existence of a second group.

Authors:  S J Steinberg; C P Ward; A H Fensom
Journal:  J Med Genet       Date:  1994-04       Impact factor: 6.318

3.  Liver and skin histopathology in adults with acid sphingomyelinase deficiency (Niemann-Pick disease type B).

Authors:  Beth L Thurberg; Melissa P Wasserstein; Thomas Schiano; Fanny O'Brien; Susan Richards; Gerald F Cox; Margaret M McGovern
Journal:  Am J Surg Pathol       Date:  2012-08       Impact factor: 6.394

Review 4.  Neural stem cell transplantation as a therapeutic approach for treating lysosomal storage diseases.

Authors:  Lamya S Shihabuddin; Seng H Cheng
Journal:  Neurotherapeutics       Date:  2011-10       Impact factor: 7.620

5.  Emerging links between pediatric lysosomal storage diseases and adult parkinsonism.

Authors:  Daniel Ysselstein; Joshua M Shulman; Dimitri Krainc
Journal:  Mov Disord       Date:  2019-02-06       Impact factor: 10.338

6.  Compound heterozygosity at the sphingomyelin phosphodiesterase-1 (SMPD1) gene is associated with low HDL cholesterol.

Authors:  Ching Yin Lee; Larbi Krimbou; Jérôme Vincent; Chantal Bernard; Pierre Larramée; Jacques Genest; Michel Marcil
Journal:  Hum Genet       Date:  2003-02-27       Impact factor: 4.132

Review 7.  Lipoprotein disorders and cardiovascular risk.

Authors:  J Genest
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

8.  Genetics of Lipid-Storage Management in Caenorhabditis elegans Embryos.

Authors:  Verena Schmökel; Nadin Memar; Anne Wiekenberg; Martin Trotzmüller; Ralf Schnabel; Frank Döring
Journal:  Genetics       Date:  2016-01-15       Impact factor: 4.562

9.  Progressive liver failure in a patient with adult Niemann-Pick disease associated with generalized AL amyloidosis.

Authors:  H Zhou; R P Linke; H E Schaefer; W Möbius; U Pfeifer
Journal:  Virchows Arch       Date:  1995       Impact factor: 4.064

10.  Sphingomyelin phosphodiesterase-1 (SMPD1) coding variants do not contribute to low levels of high-density lipoprotein cholesterol.

Authors:  Zari Dastani; Isabelle L Ruel; James C Engert; Jacques Genest; Michel Marcil
Journal:  BMC Med Genet       Date:  2007-12-18       Impact factor: 2.103

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