Literature DB >> 474720

Morphologic studies in the skeletal dysplasias.

D O Sillence, W A Horton, D L Rimoin.   

Abstract

Considerable progress has been made in the delineation of the genetic skeletal dysplasias, a heterogeneous group of disorders, that consist of over 80 distinct conditions. Morphologic studies have added a further dimension to the delineation of these conditions, their diagnosis, and the investigation of their pathogenetic mechanisms. In certain diseases, the morphologic alterations are characteristic and pathognomonic. In others only nonspecific alterations are observed, whereas in still other disorders growth-plate structure is essentially normal. Histologic, histochemical, and electronmicroscopic studies of growth-plate cartilage have provided new insights into the complexity of morphogenetic events in normal growth through the demonstration of morphologic defects in the genetic disorders of skeletal growth. As yet, very little is known of the biochemical abnormalities underlying the morphologic abnormalities. However, the great variety of morphologic findings points to a number of different pathogenetic defects in the synthesis, release, and assembly of connective tissue macromolecules and in the cells involved in growth-plate metabolism.

Entities:  

Mesh:

Year:  1979        PMID: 474720      PMCID: PMC2042401     

Source DB:  PubMed          Journal:  Am J Pathol        ISSN: 0002-9440            Impact factor:   4.307


  209 in total

1.  METAPHYSIAL DYSOSTOSIS, TYPE SCHMID.

Authors:  C E DENT; I C NORMAND
Journal:  Arch Dis Child       Date:  1964-10       Impact factor: 3.791

2.  METAPHYSEAL DYSOSTOSIS. REPORT OF FIVE FAMILIAL AND TWO SPORADIC CASES OF A MILD TYPE.

Authors:  K KOZLOWSKI
Journal:  Am J Roentgenol Radium Ther Nucl Med       Date:  1964-03

3.  DIASTROPHIC DWARFISM IN EARLY INFANCY.

Authors:  L O LANGER
Journal:  Am J Roentgenol Radium Ther Nucl Med       Date:  1965-02

4.  DWARFISM IN THE AMISH.

Authors:  V A MCKUSICK; R ELDRIDGE; J A HOSTETLER; J A EGELAND
Journal:  Trans Assoc Am Physicians       Date:  1964

5.  DWARFISM IN THE AMISH. II. CARTILAGE-HAIR HYPOPLASIA.

Authors:  V A MCKUSICK; R ELDRIDGE; J A HOSTETLER; U RUANGWIT; J A EGELAND
Journal:  Bull Johns Hopkins Hosp       Date:  1965-05

6.  HEREDITARY PROGRESSIVE ARTHRO-OPHTHALMOPATHY.

Authors:  G B STICKLER; P G BELAU; F J FARRELL; J D JONES; D G PUGH; A G STEINBERG; L E WARD
Journal:  Mayo Clin Proc       Date:  1965-06       Impact factor: 7.616

7.  A CASE OF THE SMITH-LEMLI-OPITZ SYNDROME OF MULTIPLE CONGENITAL ANOMALIES IN ASSOCIATION WITH DYSPLASIA EPIPHYSIALIS PUNCTATA.

Authors:  R GIBSON
Journal:  Can Med Assoc J       Date:  1965-03-13       Impact factor: 8.262

8.  DYSCHONDROSTEOSIS, A HEREDITABLE BONE DYSPLASIA WITH CHARACTERISTIC ROENTGENOGRAPHIC FEATURES.

Authors:  L O LANGER
Journal:  Am J Roentgenol Radium Ther Nucl Med       Date:  1965-09

9.  Substituted naphthol AS phosphate derivatives for the localization of leukocyte alkaline phosphatase activity.

Authors:  G A ACKERMAN
Journal:  Lab Invest       Date:  1962-07       Impact factor: 5.662

10.  [Asphyxiating thoracic dystrophy with familial characteristics].

Authors:  M JEUNE; C BERAUD; R CARRON
Journal:  Arch Fr Pediatr       Date:  1955
View more
  32 in total

1.  Ellis van Creveld syndrome--a report of two siblings.

Authors:  Karthik Hegde; Reema Manoj Puthran; Gopakumar Nair; Preeti P Nair
Journal:  BMJ Case Rep       Date:  2011-10-11

Review 2.  Molecular heterogeneity in chondrodysplasias.

Authors:  P H Byers
Journal:  Am J Hum Genet       Date:  1989-07       Impact factor: 11.025

3.  Quantitative histology of cartilage vascular canals in the human rib. Findings in normal neonates and children and in achondrogenesis II-hypochondrogenesis.

Authors:  H E Gruber; R S Lachman; D L Rimoin
Journal:  J Anat       Date:  1990-12       Impact factor: 2.610

4.  The ultrastructure of osteochondrosis of the articular-epiphyseal cartilage complex in growing swine.

Authors:  C S Carlson; H D Hilley; C K Henrikson; D J Meuten
Journal:  Calcif Tissue Int       Date:  1986-01       Impact factor: 4.333

5.  A new type of achondrogenesis.

Authors:  K Kozlowski; T Tsuruta; N Taki; I Tsunoda; H Ozawa; T Hasegawa; D Sillence
Journal:  Pediatr Radiol       Date:  1986

6.  Perinatally lethal short rib-polydactyly syndromes. 1. Variability in known syndromes.

Authors:  D Sillence; K Kozlowski; J Bar-ziv; A Fuhrumann-Rieger; W Fuhrmann; F Pascu
Journal:  Pediatr Radiol       Date:  1987

7.  Atelosteogenesis: evidence for heterogeneity.

Authors:  D O Sillence; K Kozlowski; J G Rogers; P L Sprague; G J Cullity; R A Osborn
Journal:  Pediatr Radiol       Date:  1987

8.  Association of spondylo-epiphyseal dysplasia with nephrotic syndrome.

Authors:  J H Ehrich; G Offner; E Schirg; P F Hoyer; U Helmchen; J Brodehl
Journal:  Pediatr Nephrol       Date:  1990-03       Impact factor: 3.714

9.  Assembly of cartilage collagen fibrils is disrupted by overexpression of normal type II collagen in transgenic mice.

Authors:  S Garofalo; M Metsäranta; J Ellard; C Smith; W Horton; E Vuorio; B de Crombrugghe
Journal:  Proc Natl Acad Sci U S A       Date:  1993-05-01       Impact factor: 11.205

10.  Amino acid substitutions of conserved residues in the carboxyl-terminal domain of the alpha 1(X) chain of type X collagen occur in two unrelated families with metaphyseal chondrodysplasia type Schmid.

Authors:  G A Wallis; B Rash; W A Sweetman; J T Thomas; M Super; G Evans; M E Grant; R P Boot-Handford
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.