Literature DB >> 2744018

Study of the bone pathology in early mucolipidosis II (I-cell disease).

U E Pazzaglia1, G Beluffi, E Bianchi, A Castello, A Coci, A Marchi.   

Abstract

Histological examination of the bones obtained on autopsy of a 5-month-old child with mucolipidosis II (I-cell disease) revealed inhibition of the growth plate calcification with defective vascular invasion and signs of hyperparathyroidism. These findings are the chondro-osseous basis of the early radiological ricket-like appearance of bones in the neonatal period or soon thereafter. Whether the early skeletal abnormalities of mucolipidosis II result from a primary enzymatic defect of cartilage and bone cells or from factors controlling bone metabolism deserves further study.

Entities:  

Mesh:

Year:  1989        PMID: 2744018     DOI: 10.1007/bf00441557

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  9 in total

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

Authors:  J J Martin; J G Leroy; J P Farriaux; G Fontaine; R J Desnick; A Cabello
Journal:  Acta Neuropathol       Date:  1975-12-30       Impact factor: 17.088

2.  Fetal mucolipidosis II (I-cell disease): radiologic and pathologic correlation.

Authors:  D S Babcock; K E Bove; G Hug; P S Dignan; S Soukup; N S Warren
Journal:  Pediatr Radiol       Date:  1986

3.  I-cell disease, mucolipidosis II. Pathological, histochemical, ultrastructural and biochemical observations in four cases.

Authors:  E F Gilbert; G Dawson; G M zu Rhein; J M Opitz
Journal:  Z Kinderheilkd       Date:  1973

4.  A hypothesis for I-cell disease: defective hydrolases that do not enter lysosomes.

Authors:  S Hickman; E F Neufeld
Journal:  Biochem Biophys Res Commun       Date:  1972-11-15       Impact factor: 3.575

5.  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

6.  Roentgenographic manifestations of Leroy's I-cell disease.

Authors:  P Taber; M T Gyepes; M Philippart; S Ling
Journal:  Am J Roentgenol Radium Ther Nucl Med       Date:  1973-05

7.  I-cell disease. Report of three cases.

Authors:  Y Terashima; K Tsuda; S Isomura; Y Sugiura; H Nogami
Journal:  Am J Dis Child       Date:  1975-09

8.  Neonatal mucolipidosis II (I-cell disease): clinical and radiologic features in three cases.

Authors:  H B Patriquin; P Kaplan; H P Kind; A Giedion
Journal:  AJR Am J Roentgenol       Date:  1977-07       Impact factor: 3.959

9.  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
  9 in total
  8 in total

1.  The natural history and osteodystrophy of mucolipidosis types II and III.

Authors:  Grace David-Vizcarra; Julie Briody; Jenny Ault; Michael Fietz; Janice Fletcher; Ravi Savarirayan; Meredith Wilson; Jim McGill; Matthew Edwards; Craig Munns; Melanie Alcausin; Sara Cathey; David Sillence
Journal:  J Paediatr Child Health       Date:  2010-03-29       Impact factor: 1.954

2.  Term Neonate Presenting with the Combined Occurrence of Mucolipidosis Type II and Leigh Syndrome.

Authors:  Rebecca R Speer; Uzoamaka C Ezeanya; Sarah J Beaudoin; Kristen M Glass; Christiana N Oji-Mmuo
Journal:  J Pediatr Genet       Date:  2019-10-24

3.  A novel intermediate mucolipidosis II/IIIαβ caused by GNPTAB mutation in the cytosolic N-terminal domain.

Authors:  Jules G Leroy; David Sillence; Tim Wood; Jarrod Barnes; Robert Roger Lebel; Michael J Friez; Roger E Stevenson; Richard Steet; Sara S Cathey
Journal:  Eur J Hum Genet       Date:  2013-09-18       Impact factor: 4.246

4.  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

5.  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

6.  Primary hyperparathyroidism: an overview.

Authors:  Jessica Mackenzie-Feder; Sandra Sirrs; Donald Anderson; Jibran Sharif; Aneal Khan
Journal:  Int J Endocrinol       Date:  2011-06-02       Impact factor: 3.257

7.  I-Cell Disease (Mucolipidosis II) Presenting as Neonatal Fractures: A Case for Continued Monitoring of Serum Parathyroid Hormone Levels.

Authors:  Aneal Khan; Josephine Ho; Amy Pender; Xingchang Wei; Murray Potter
Journal:  Clin Pediatr Endocrinol       Date:  2008-08-08

8.  Elevated Bone Turnover in an Infantile Patient with Mucolipidosis II; No Association with Hyperparathyroidism.

Authors:  Takanobu Otomo; Takehisa Yamamoto; Yasuhiro Fujikawa; Tsunesuke Shimotsuji; Keiichi Ozono
Journal:  Clin Pediatr Endocrinol       Date:  2011-03-26
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.