Literature DB >> 514691

Kniest dysplasia. A histochemical study of the growth plate.

W A Horton, D L Rimoin.   

Abstract

Chondro-osseous tissue from four patients with the Kniest dysplasia was studied histochemically using a new plastic embedding technique. Extensive vacuolar changes were observed p--1 throughout the endochondral growth plate and adjacent resting cartilage. These changes occurred within the cartilage matrix and also in the lacunae of degenerating chrondrocytes. The septa of the lesions contained chondroitin sulfate, but little keratan sulfate or collagen. Resting cartilage not adjacent to the growth plate stained irregularly and showed few of the vacuolar lesions, and chondrocytes were enlarged and contained cytoplasic inclusions, but no vacuolar material. Thus, there appears to be a sequence of events initiated by cellular accumulation of a substance and progressing to cellular and matrix degeneration.

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Year:  1979        PMID: 514691     DOI: 10.1203/00006450-197911000-00012

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  4 in total

1.  Kniest dysplasia: MR correlation of histologic and radiographic peculiarities.

Authors:  Jerry R Dwek
Journal:  Pediatr Radiol       Date:  2004-08-26

2.  The deletion of six amino acids at the C-terminus of the alpha 1 (II) chain causes overmodification of type II and type XI collagen: further evidence for the association between small deletions in COL2A1 and Kniest dysplasia.

Authors:  A Winterpacht; A Superti-Furga; U Schwarze; H Stöss; B Steinmann; J Spranger; B Zabel
Journal:  J Med Genet       Date:  1996-08       Impact factor: 6.318

3.  Expression, in cartilage, of a 7-amino-acid deletion in type II collagen from two unrelated individuals with Kniest dysplasia.

Authors:  R Bogaert; D Wilkin; W R Wilcox; R Lachman; D Rimoin; D H Cohn; D R Eyre
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025

4.  Kniest dysplasia is characterized by an apparent abnormal processing of the C-propeptide of type II cartilage collagen resulting in imperfect fibril assembly.

Authors:  A R Poole; I Pidoux; A Reiner; L Rosenberg; D Hollister; L Murray; D Rimoin
Journal:  J Clin Invest       Date:  1988-02       Impact factor: 14.808

  4 in total

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