Literature DB >> 11316691

Isolated splenomegaly as the presenting feature of Niemann-Pick disease type C.

J Imrie1, J E Wraith.   

Abstract

WE DESCRIBE FOUR PATIENTS WITH NIEMANN: Pick disease type C (NPC), in whom the presentation was isolated splenic enlargement; this remained the only abnormality for a number of years. Diagnosis can be suggested by either finding abnormal storage material in a tissue biopsy specimen or by showing a modest elevation in plasma chitotriosidase activity. In patients with suggestive abnormalities, filipin staining of a skin fibroblast sample should confirm the abnormality in cholesterol trafficking. Formal esterification studies and mutation analysis should also be performed, especially if prenatal testing is to be performed in subsequent pregnancies. If the diagnosis is not considered and established, the family are at risk of having further affected children. Investigation of patients with isolated splenomegaly is not complete until NPC has been excluded.

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Year:  2001        PMID: 11316691      PMCID: PMC1718763          DOI: 10.1136/adc.84.5.427

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  12 in total

1.  An adult with a non-neuronopathic form of Niemann-Pick C disease.

Authors:  A H Fensom; A R Grant; S J Steinberg; C P Ward; B D Lake; E C Logan; G Hulman
Journal:  J Inherit Metab Dis       Date:  1999-02       Impact factor: 4.982

2.  Prenatal diagnosis of Niemann-Pick type C disease: current strategy from an experience of 37 pregnancies at risk.

Authors:  M T Vanier; C Rodriguez-Lafrasse; R Rousson; G Mandon; J Boué; A Choiset; M F Peyrat; C Dumontel; M C Juge; P G Pentchev
Journal:  Am J Hum Genet       Date:  1992-07       Impact factor: 11.025

3.  Niemann-Pick disease type C (a cellular cholesterol lipidosis) treated by bone marrow transplantation.

Authors:  Y S Hsu; W L Hwu; S F Huang; M Y Lu; R L Chen; D T Lin; S S Peng; K H Lin
Journal:  Bone Marrow Transplant       Date:  1999-07       Impact factor: 5.483

4.  Niemann-Pick C1 disease: the I1061T substitution is a frequent mutant allele in patients of Western European descent and correlates with a classic juvenile phenotype.

Authors:  G Millat; C Marçais; M A Rafi; T Yamamoto; J A Morris; P G Pentchev; K Ohno; D A Wenger; M T Vanier
Journal:  Am J Hum Genet       Date:  1999-11       Impact factor: 11.025

5.  A progressive neurologic disorder with supranuclear vertical gaze paresis and distinctive bone marrow cells.

Authors:  F L Yan-Go; T Yanagihara; R V Pierre; N P Goldstein
Journal:  Mayo Clin Proc       Date:  1984-06       Impact factor: 7.616

6.  A defect in cholesterol esterification in Niemann-Pick disease (type C) patients.

Authors:  P G Pentchev; M E Comly; H S Kruth; M T Vanier; D A Wenger; S Patel; R O Brady
Journal:  Proc Natl Acad Sci U S A       Date:  1985-12       Impact factor: 11.205

7.  A neurovisceral storage disease with vertical supranuclear ophthalmoplegia, and its relationship to Niemann-Pick disease. A report of nine patients.

Authors:  B G Neville; B D Lake; R Stephens; M D Sanders
Journal:  Brain       Date:  1973       Impact factor: 13.501

8.  Clinical spectrum of Niemann-Pick disease type C.

Authors:  J K Fink; M R Filling-Katz; J Sokol; D G Cogan; A Pikus; B Sonies; B Soong; P G Pentchev; M E Comly; R O Brady
Journal:  Neurology       Date:  1989-08       Impact factor: 9.910

9.  Niemann-Pick C1 protein: obligatory roles for N-terminal domains and lysosomal targeting in cholesterol mobilization.

Authors:  H Watari; E J Blanchette-Mackie; N K Dwyer; J M Glick; S Patel; E B Neufeld; R O Brady; P G Pentchev; J F Strauss
Journal:  Proc Natl Acad Sci U S A       Date:  1999-02-02       Impact factor: 11.205

10.  Niemann-Pick disease type C: nodular splenomegaly.

Authors:  L P Omarini; S E Frank-Burkhardt; T A Seemayer; G Mentha; F Terrier
Journal:  Abdom Imaging       Date:  1995 Mar-Apr
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  8 in total

1.  Critical assessment of chitotriosidase analysis in the rational laboratory diagnosis of children with Gaucher disease and Niemann-Pick disease type A/B and C.

Authors:  Markus Ries; Ellen Schaefer; Till Lührs; Latha Mani; Jana Kuhn; Marie T Vanier; Frank Krummenauer; Andreas Gal; Michael Beck; Eugen Mengel
Journal:  J Inherit Metab Dis       Date:  2006-07-27       Impact factor: 4.982

2.  Niemann-Pick disease type C in the newborn period: a single-center experience.

Authors:  Ersin Gumus; Goknur Haliloglu; Asuman Nur Karhan; Hulya Demir; Figen Gurakan; Meral Topcu; Aysel Yuce
Journal:  Eur J Pediatr       Date:  2017-09-27       Impact factor: 3.183

3.  Long-term efficacy of miglustat in paediatric patients with Niemann-Pick disease type C.

Authors:  Y H Chien; S F Peng; C C Yang; N C Lee; L K Tsai; A C Huang; S C Su; C C Tseng; W L Hwu
Journal:  J Inherit Metab Dis       Date:  2012-04-05       Impact factor: 4.982

Review 4.  Niemann-Pick disease type C.

Authors:  Marie T Vanier
Journal:  Orphanet J Rare Dis       Date:  2010-06-03       Impact factor: 4.123

Review 5.  Recent advances in the diagnosis and treatment of niemann-pick disease type C in children: a guide to early diagnosis for the general pediatrician.

Authors:  Hanna Alobaidy
Journal:  Int J Pediatr       Date:  2015-02-16

6.  Elevated granulocyte-colony stimulating factor and hematopoietic stem cell mobilization in Niemann-Pick type C1 disease.

Authors:  Anouk G Groenen; Anouk M La Rose; Mengying Li; Venetia Bazioti; Arthur F Svendsen; Niels J Kloosterhuis; Albertina Ausema; Alle Pranger; M Rebecca Heiner-Fokkema; Klary E Niezen-Koning; Tom Houben; Ronit Shiri-Sverdlov; Marit Westerterp
Journal:  J Lipid Res       Date:  2022-01-08       Impact factor: 5.922

7.  Disease and patient characteristics in NP-C patients: findings from an international disease registry.

Authors:  Marc C Patterson; Eugen Mengel; Frits A Wijburg; Audrey Muller; Barbara Schwierin; Harir Drevon; Marie T Vanier; Mercé Pineda
Journal:  Orphanet J Rare Dis       Date:  2013-01-16       Impact factor: 4.123

Review 8.  Niemann-Pick disease type C symptomatology: an expert-based clinical description.

Authors:  Eugen Mengel; Hans-Hermann Klünemann; Charles M Lourenço; Christian J Hendriksz; Frédéric Sedel; Mark Walterfang; Stefan A Kolb
Journal:  Orphanet J Rare Dis       Date:  2013-10-17       Impact factor: 4.123

  8 in total

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