Literature DB >> 6803579

Growth curves for height for diastrophic dysplasia, spondyloepiphyseal dysplasia congenita, and pseudoachondroplasia.

W A Horton, J G Hall, C I Scott, R E Pyeritz, D L Rimoin.   

Abstract

Analysis of retrospective growth data from 72 patients with diastrophic dysplasia, 62 patients with spondyloepiphyseal dysplasia congenita and 61 patients with pseudoachondroplasia permitted the establishment of preliminary reference growth standards for height for each disorder. In addition, a comparison of mean height curves for these three disorders and achondroplasia revealed dissimilarities in growth patterns.

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Mesh：

Year:  1982        PMID： 6803579     DOI： 10.1001/archpedi.1982.03970400034010

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN： 0002-922X


  12 in total

Review 1.  Development of pseudo-achondroplasia over a 30-year period in an adult patient.

Authors:  J M Nores; P Maroteaux; J M Remy
Journal:  Clin Rheumatol       Date:  1989-06       Impact factor: 2.980

Review 2.  Special growth charts.

Authors:  J A Hulse
Journal:  Arch Dis Child       Date:  1988-10       Impact factor: 3.791

3.  Severe pseudoachondroplasia with parental consanguinity.

Authors:  I D Young; J R Moore
Journal:  J Med Genet       Date:  1985-04       Impact factor: 6.318

4.  Analysis of the chondroitin sulfate proteoglycan core protein (CSPGCP) gene in achondroplasia and pseudoachondroplasia.

Authors:  J E Finkelstein; K Doege; Y Yamada; R E Pyeritz; J M Graham; J B Moeschler; R M Pauli; J T Hecht; C A Francomano
Journal:  Am J Hum Genet       Date:  1991-01       Impact factor: 11.025

Review 5.  The weight of the fourth dimension for the diagnosis of genetic bone disease.

Authors:  A Giedion
Journal:  Pediatr Radiol       Date:  1994

Review 6.  Cartilage oligomeric matrix protein: COMPopathies and beyond.

Authors:  Karen L Posey; Francoise Coustry; Jacqueline T Hecht
Journal:  Matrix Biol       Date:  2018-03-09       Impact factor: 11.583

Review 7.  The value of the study of natural history in genetic disorders and congenital anomaly syndromes.

Authors:  J G Hall
Journal:  J Med Genet       Date:  1988-07       Impact factor: 6.318

8.  Pseudoachondroplasia: clinical diagnosis at different ages and comparison of autosomal dominant and recessive types. A review of 32 patients (26 kindreds).

Authors:  R Wynne-Davies; C M Hall; I D Young
Journal:  J Med Genet       Date:  1986-10       Impact factor: 6.318

9.  The clinical features of spondyloepiphyseal dysplasia congenita resulting from the substitution of glycine 997 by serine in the alpha 1(II) chain of type II collagen.

Authors:  W G Cole; R K Hall; J G Rogers
Journal:  J Med Genet       Date:  1993-01       Impact factor: 6.318

10.  Type II collagen defects in the chondrodysplasias. I. Spondyloepiphyseal dysplasias.

Authors:  L W Murray; J Bautista; P L James; D L Rimoin
Journal:  Am J Hum Genet       Date:  1989-07       Impact factor: 11.025
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