Literature DB >> 3084

I-cell disease (mucolipidosis II):a report on its pathology.

J J Martin, J G Leroy, J P Farriaux, G Fontaine, R J Desnick, A Cabello.   

Abstract

The single most characteristic morphological feature in I-cell disease (ICD) is the accumulation of membrane-bound vacuoles in mesenchymal cells (mainly fibroblasts). No true storage can be documented in those vacuoles. That their contents could have been dissolved during fixation or embedding remains however a possibility. Remnants consisting of a few lamellar arrays and of small amounts of fibrillo-granular material are too scarce for histochemical characterization. In hepatocytes large cells in the white pulp of the spleen and in myocardial fibers, vacuoles with fixative insoluble contents have been discovered; they are nowhere very abundant and their specificity is questionable. Because the affected fibroblastic elements represent a small fraction in any organ, most secondary biochemical abnormalities are expected to be detectable only in purely fibroblastic tissues. Our pathological study contributes to the understanding of some of the clinical features characteristic of ICD and stresses major morphological differences between ICD and the many diseases classified as mucopolysaccharidoses and mucolipidoses.

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Year:  1975        PMID: 3084     DOI: 10.1007/BF00686161

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  34 in total

1.  A recognition marker required for uptake of a lysosomal enzyme by cultured fibroblasts.

Authors:  S Hickman; L J Shapiro; E F Neufeld
Journal:  Biochem Biophys Res Commun       Date:  1974-03-15       Impact factor: 3.575

2.  [A rare atypical muscular inclusion: "fingerprint bodies" (author's transl)].

Authors:  A Sengel; P Stoebner
Journal:  Acta Neuropathol       Date:  1974-02-07       Impact factor: 17.088

3.  "I-cell" disease: leakage of lysosomal enzymes into extracellular fluids.

Authors:  U Wiesmann; F Vassella; N Herschkowitz
Journal:  N Engl J Med       Date:  1971-11-04       Impact factor: 91.245

4.  Clinical, biochemical, and ultrastructural studies in a case of chondrodystrophy presenting the I-cell phenotype in tissue culture.

Authors:  M Tondeur; E Vamos-Hurwitz; S Mockel-Pohl; J P Dereume; N Cremer; H Loeb
Journal:  J Pediatr       Date:  1971-09       Impact factor: 4.406

5.  Ultrastructure and function of eccrine glands in the mucopolysaccharidoses.

Authors:  R W Belcher
Journal:  Arch Pathol       Date:  1973-11

6.  [Mucolipidosis type II (inclusion cell disease). Study of a case and review of the literature].

Authors:  G de Montis; P Garnier; N Thomassin; J C Job; A Rossier
Journal:  Ann Pediatr (Paris)       Date:  1972-05-02

7.  Multiple lysosomal enzyme deficiency due to enzyme leakage?

Authors:  U N Wiesmann; J Lightbody; F Vassella; N N Herschkowitz
Journal:  N Engl J Med       Date:  1971-01-14       Impact factor: 91.245

8.  Diagnosis of glycosphingolipidoses by urinary-sediment analysis.

Authors:  R J Desnick; G Dawson; S J Desnick; C C Sweeley; W Krivit
Journal:  N Engl J Med       Date:  1971-04-08       Impact factor: 91.245

9.  The precipitation of polyanions by long-chain aliphatic ammonium compounds. IV. Elution in salt solutions of mucopolysaccharide-quaternary ammonium complexes adsorbed on a support.

Authors:  C A ANTONOPOULOS; E BORELIUS; S GARDELL; B HAMNSTROM; J E SCOTT
Journal:  Biochim Biophys Acta       Date:  1961-12-09

10.  I-cell disease (mucolipidosis type II). Serum hydrolases in obligate heterozygotes.

Authors:  J G Leroy; A F Van Elsen
Journal:  Humangenetik       Date:  1973
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  16 in total

Review 1.  Delineating the role of alterations in lipid metabolism to the pathogenesis of inherited skeletal and cardiac muscle disorders: Thematic Review Series: Genetics of Human Lipid Diseases.

Authors:  Harjot K Saini-Chohan; Ryan W Mitchell; Frédéric M Vaz; Teresa Zelinski; Grant M Hatch
Journal:  J Lipid Res       Date:  2011-11-07       Impact factor: 5.922

2.  Dominant inheritance of sialuria, an inborn error of feedback inhibition.

Authors:  J G Leroy; R Seppala; M Huizing; G Dacremont; H De Simpel; R N Van Coster; E Orvisky; D M Krasnewich; W A Gahl
Journal:  Am J Hum Genet       Date:  2001-04-18       Impact factor: 11.025

3.  Asymmetric ventricular septal hypertrophy in I-cell disease.

Authors:  N Sakura; M Hayashida; C Waki; M Kobayashi; T Tanimoto
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

4.  Menkes kinky-hair disease. A report on its pathology.

Authors:  J J Martin; J Flament-Durand; J P Farriaux; N Buyssens; P Ketelbant-Balasse; C Jansen
Journal:  Acta Neuropathol       Date:  1978-04-26       Impact factor: 17.088

Review 5.  Proteinuria in a child with sialidosis: case report and histological studies.

Authors:  C E Kashtan; T E Nevins; Z Posalaky; R L Vernier; A J Fish
Journal:  Pediatr Nephrol       Date:  1989-04       Impact factor: 3.714

6.  Retarded bone formation in GM1-gangliosidosis: a study of the infantile form and comparison with two canine models.

Authors:  J Alroy; K Knowles; S H Schelling; E M Kaye; A E Rosenberg
Journal:  Virchows Arch       Date:  1995       Impact factor: 4.064

7.  Altered chondrocyte differentiation and extracellular matrix homeostasis in a zebrafish model for mucolipidosis II.

Authors:  Heather Flanagan-Steet; Christina Sias; Richard Steet
Journal:  Am J Pathol       Date:  2009-10-15       Impact factor: 4.307

8.  Phenotype and genotype in mucolipidoses II and III alpha/beta: a study of 61 probands.

Authors:  S S Cathey; J G Leroy; T Wood; K Eaves; R J Simensen; M Kudo; R E Stevenson; M J Friez
Journal:  J Med Genet       Date:  2009-07-16       Impact factor: 6.318

9.  I-cell disease. A further report on its pathology.

Authors:  J J Martin; J G Leroy; M van Eygen; C Ceuterick
Journal:  Acta Neuropathol       Date:  1984       Impact factor: 17.088

10.  Radiological signs of mucolipidosis II or I-cell disease. A study of nine cases.

Authors:  L Lemaitre; J Remy; J P Farriaux; J L Dhondt; R Walbaum
Journal:  Pediatr Radiol       Date:  1978-06-19
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