Literature DB >> 11405334

Changes in clinical practice with the unravelling of diseases: connective-tissue disorders.

J Spranger1.   

Abstract

Unravelling of diseases is achieved in steps by sequentially describing their phenotype, natural course, aetiology and pathogenesis. Through succinct clinical observation, conglomerates of heterogeneous connective-tissue disorders, such as various forms of disproportionate dwarfism, have been split into well-defined entities. They have often been confirmed by biochemical and molecular analysis. On the other hand, seemingly disparate disorders have been shown to be pathogenetically related and to be variable expressions of common defects. Examples are the mucopolysaccharidoses and type II collagenopathies. Disease recognition through splitting and lumping has improved prevention and prognostication. It is the basic requirement for future therapeutic attempts on a pathogenetic or molecular level.

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Year:  2001        PMID: 11405334     DOI: 10.1023/a:1010354614926

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  21 in total

1.  Clinical and radiographic features of a family with hypochondroplasia owing to a novel Asn540Ser mutation in the fibroblast growth factor receptor 3 gene.

Authors:  G Mortier; L Nuytinck; M Craen; J P Renard; J G Leroy; A de Paepe
Journal:  J Med Genet       Date:  2000-03       Impact factor: 6.318

2.  Clinical and biochemical manifestations of hyaluronidase deficiency.

Authors:  M R Natowicz; M P Short; Y Wang; G R Dickersin; M C Gebhardt; D I Rosenthal; K B Sims; A E Rosenberg
Journal:  N Engl J Med       Date:  1996-10-03       Impact factor: 91.245

3.  Common mutations in the fibroblast growth factor receptor 3 (FGFR 3) gene account for achondroplasia, hypochondroplasia, and thanatophoric dwarfism.

Authors:  J Bonaventure; F Rousseau; L Legeai-Mallet; M Le Merrer; A Munnich; P Maroteaux
Journal:  Am J Med Genet       Date:  1996-05-03

Review 4.  The type II collagenopathies: a spectrum of chondrodysplasias.

Authors:  J Spranger; A Winterpacht; B Zabel
Journal:  Eur J Pediatr       Date:  1994-02       Impact factor: 3.183

5.  Mutations in CDMP1 cause autosomal dominant brachydactyly type C.

Authors:  A Polinkovsky; N H Robin; J T Thomas; M Irons; A Lynn; F R Goodman; W Reardon; S G Kant; H G Brunner; I van der Burgt; D Chitayat; J McGaughran; D Donnai; F P Luyten; M L Warman
Journal:  Nat Genet       Date:  1997-09       Impact factor: 38.330

6.  Disruption of human limb morphogenesis by a dominant negative mutation in CDMP1.

Authors:  J T Thomas; M W Kilpatrick; K Lin; L Erlacher; P Lembessis; T Costa; P Tsipouras; F P Luyten
Journal:  Nat Genet       Date:  1997-09       Impact factor: 38.330

7.  A severe autosomal recessive acromesomelic dysplasia, the Hunter-Thompson type, and comparison with the Grebe type.

Authors:  L O Langer; J Cervenka; M Camargo
Journal:  Hum Genet       Date:  1989-03       Impact factor: 4.132

8.  Genetic heterogeneity in osteogenesis imperfecta.

Authors:  D O Sillence; A Senn; D M Danks
Journal:  J Med Genet       Date:  1979-04       Impact factor: 6.318

9.  Acromesomelic dwarfism: description of a patient and comparison with previously reported cases.

Authors:  A G Hunter; M W Thompson
Journal:  Hum Genet       Date:  1976-09-10       Impact factor: 4.132

10.  Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia.

Authors:  F Rousseau; J Bonaventure; L Legeai-Mallet; A Pelet; J M Rozet; P Maroteaux; M Le Merrer; A Munnich
Journal:  Nature       Date:  1994-09-15       Impact factor: 49.962

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  1 in total

1.  Reduction Mammaplasty in a Patient with Kniest Dysplasia: Case Report and Literature Review.

Authors:  Trajan A Cuellar; Jessica Erdmann-Sager
Journal:  Plast Reconstr Surg Glob Open       Date:  2020-03-25
  1 in total

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