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chondrodystrophy

Known as: Cartilage Development Disorder, DISORDER CARTILAGE DEVELOPMENT (NOS), chondrodystrophies 
Any dysfunction in the growth of cartilage.
National Institutes of Health

Related topics

Related topics

16 relations
AchondrogenesisChondrodysplasiaConnective and Soft TissueHereditary Multiple Exostoses

Broader (4)

Bone Diseases, DevelopmentalCartilage DiseasesFetal DiseasesMusculoskeletal Diseases

Narrower (1)

Chondrodysplasia Punctata

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2010
2010
Mycoplasma iowae associated with chondrodystrophy in commercial turkeys
Opportunistic observations of and necropsies from selected commercial (meat) turkey flocks revealed skeletal lesions consistent… 
Highly Cited
2003
Highly Cited
2003
Autosomal recessive HEM/Greenberg skeletal dysplasia is caused by 3 beta-hydroxysterol delta 14-reductase deficiency due to mutations in the lamin B receptor gene.
Hydrops-ectopic calcification-"moth-eaten" (HEM) or Greenberg skeletal dysplasia is an autosomal recessive chondrodystrophy with… 
1994
1994
The chondrodystrophy, nanomelia: biosynthesis and processing of the defective aggrecan precursor.
The lethal chicken mutation nanomelia leads to severe skeletal defects because of a deficiency of aggrecan, which is the largest… 
1977
1977
Developmental abnormalities of the occipital bone in human chondrodystrophies (achondroplasia and thanatophoric dwarfism).
Specific developmental malformations have been demonstrated in the occipital bone of two chondrodysplastic disorders… 
1976
1976
Intracytoplasmic inclusion bodies in the chondrocytes of type I lethal achondrogenesis.
1975
1975
Chondrodystrophy: an inherited lethal condition in turkey embryos.
Chondrodystrophy was found to occur as an embryonic lethal in a special line of turkeys. Inheritance of the condition was studied… 
1971
1971
Asphyxiating thoracic chondrodystrophy. Association with renal disease and evidence for possile heterozygous expression.
Asphyxiating thoracic dystrophy of the newborn is a rare skeletal abnormality. 
1955
1955
Comments on the rate of mutation to chondrodystrophy in man.
RECENT studies of the rate of mutation at various loci in man, a summary of which may be found in the paper by Neel and Falls… 
1953
1953
Chondrodystrophy with Ectodermal Defects
M.H., the elder of two girls, first came under observation by one of us (EJ.G.) in 1943 because of multiple orthopaedic… 
1937
1937
Cretinoid epiphyseal dysgenesis
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