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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
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Related topics
Related topics
16 relations
Achondrogenesis
Chondrodysplasia
Connective and Soft Tissue
Hereditary Multiple Exostoses
Expand
Broader (4)
Bone Diseases, Developmental
Cartilage Diseases
Fetal Diseases
Musculoskeletal 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
David H. Ley
,
R. Marusak
,
Eduardo J. Vivas
,
H. John Barnes
,
Oscar J. Fletcher
Avian Pathology
2010
Corpus ID: 39269901
Opportunistic observations of and necropsies from selected commercial (meat) turkey flocks revealed skeletal lesions consistent…
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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.
H. Waterham
,
J. Koster
,
+6 authors
J. Oosterwijk
American Journal of Human Genetics
2003
Corpus ID: 5680802
Hydrops-ectopic calcification-"moth-eaten" (HEM) or Greenberg skeletal dysplasia is an autosomal recessive chondrodystrophy with…
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1999
1999
The toothless osteopetrotic rat has a normal vitamin D-binding protein-macrophage activating factor (DBP-MAF) cascade and chondrodysplasia resistant to treatments with colony stimulating factor-1…
P. Odgren
,
S. Popoff
,
+4 authors
S. Marks,
Bone
1999
Corpus ID: 78733
1994
1994
The chondrodystrophy, nanomelia: biosynthesis and processing of the defective aggrecan precursor.
B. Vertel
,
B. Grier
,
Haoxiang Lit
,
Nancy B. SCHWARTZt
Biochemical Journal
1994
Corpus ID: 23021552
The lethal chicken mutation nanomelia leads to severe skeletal defects because of a deficiency of aggrecan, which is the largest…
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1977
1977
Developmental abnormalities of the occipital bone in human chondrodystrophies (achondroplasia and thanatophoric dwarfism).
M. Marín‐padilla
,
T. M. Marin-Padilla
Birth defects original article series
1977
Corpus ID: 27579628
Specific developmental malformations have been demonstrated in the occipital bone of two chondrodysplastic disorders…
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1976
1976
Intracytoplasmic inclusion bodies in the chondrocytes of type I lethal achondrogenesis.
S. Yang
,
K. Heidelberger
,
J. Bernstein
Human Pathology
1976
Corpus ID: 36025427
1975
1975
Chondrodystrophy: an inherited lethal condition in turkey embryos.
L. Gaffney
Journal of Heredity
1975
Corpus ID: 10383138
Chondrodystrophy was found to occur as an embryonic lethal in a special line of turkeys. Inheritance of the condition was studied…
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1971
1971
Asphyxiating thoracic chondrodystrophy. Association with renal disease and evidence for possile heterozygous expression.
M. Shokeir
,
C. Houston
,
C. Awen
Journal of Medical Genetics
1971
Corpus ID: 30909237
Asphyxiating thoracic dystrophy of the newborn is a rare skeletal abnormality.
1953
1953
Chondrodystrophy with Ectodermal Defects
Ectodermal Defects
,
E. Gallagher
,
M. Macgregor
,
M. Israelski
Archives of Disease in Childhood
1953
Corpus ID: 10517349
M.H., the elder of two girls, first came under observation by one of us (EJ.G.) in 1943 because of multiple orthopaedic…
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1937
1937
Cretinoid epiphyseal dysgenesis
W. A. Reilly
,
F. Smyth
1937
Corpus ID: 72700549
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