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  • ¿µ¹®
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  • chondrogenesis
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  • chondrogenic layer
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  • chondrogladiolar
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  • chondroglossus muscle
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  • chondroid
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  • chondroid syringoma
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  • chondroitin sulfate
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  • chondrolipoma
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  • chondrology
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  • chondrolysis
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  • chondroma
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  • chondromalacia
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  • chondromatosis
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  • chondrometaplasia
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  • chondromucosal flap
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  • ¿µ¹®
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  • chondrogenic zone
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  • chondrogladiolar
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  • chondroglossus muscle
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  • chondroid
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  • chondroid syringoma
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  • chondroitin sulfate
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  • chondrology
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  • chondrolysis
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  • chondroma
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  • chondromalacia
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  • chondromatosis
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  • chondrometaplasia
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  • chondromucosal flap
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  • chondromyxoid fibroma
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  • chondropathia
    (¢¡chondropathy) ¿¬°ñº´Áõ
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  • ¿µ¹®
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  • chondrodysplasia
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  • chondrodysplasia punctata
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  • chondrodystrophia calcificans congenita
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  • chondrodystrophia<³ª>
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  • chondrodystrophy
    ¿¬°ñ ÀÌ¿µ¾çÁõ (æãÍéì¶ç½å×ñø).
  • chondroectodermal dysplasia
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  • chondrogen
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  • chondrogen
    Äܵå·Î°Õ, ¿¬°ñ¿ø(æãÍéê«).
  • chondrogenesis
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  • chondrogenesis
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  • chondrogenic layer
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  • chondrogenic zone
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  • chondroglossus
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  • chondroglossus m.
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  • chondroid
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  • ÄÚµå
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  • M22.4
    Chondromalacia patellae
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  • chondromyxoid fibroma
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  • chondromyxosarcoma
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    À°Á¾°ú ¿¬°ñ ¼ººÐÀ» °®´Â ¾Ç¼º °£¿±Á¾.
  • chondropharyngeal part
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  • chondroplasia
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  • chondroplasty
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  • chondrosarcoma
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  • chondrosternoplasty
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chondrodynia <symptom> Pain in and around cartilage.
(15 Jan 1998)
chondrodysplasia <embryology, orthopaedics> A disturbance in the development of cartilage, primarily the long bones. This can result in arrested growth and dwarfism.
Origin: Gr. Plassein = to form
(15 Jan 1998)
chondrodysplasia punctata A heterogeneous group of bone dysplasias, the common character of which is stippling of the epiphyses in infancy. The group includes a severe autosomal recessive form (chondrodysplasia punctata, rhizomelic), an autosomal dominant form (conradi-hunermann syndrome), and a milder x-linked form. Metabolic defects associated with impaired peroxisomes are present only in the rhizomelic form.
(12 Dec 1998)
chondrodysplasia punctata, rhizomelic An autosomal recessive form of chondrodysplasia punctata characterised by defective plasmalogen biosynthesis and impaired peroxisomes. Patients have shortened proximal limbs and severely disturbed endochondrial bone formation. The metabolic defects associated with the impaired peroxisomes are present only in the rhizomelic form of chondrodysplasia punctata.
(12 Dec 1998)
chondrodystrophia <embryology, orthopaedics> A disturbance in the development of cartilage, primarily the long bones. This can result in arrested growth and dwarfism.
(15 Jan 1998)
chondrodystrophia calcificans congenita A developmental error of the epiphyses characterised by severe deformities, epiphyses ossified from several discrete centres and with a stippled appearance, and thickened shafts of the long bones; congenital cataract and mental retardation are often present. There is an autosomal dominant form and an autosomal recessive form.
Synonym: chondrodysplasia punctata, chondrodystrophia calcificans congenita, hypoplastic foetal chondrodystrophy, stippled epiphysis.
(05 Mar 2000)
chondrodystrophia congenita punctata Congenital shortening of the humerus and femur, with stippled epiphyses, high-arched palate, cataracts, erythroderma in the newborn, and scaling followed by follicular atrophoderma; there is also an autosomal dominant inheritance pattern .
Synonym: chondrodystrophia congenita punctata.
(05 Mar 2000)
chondrodystrophic dwarfism See: chondrodystrophy.
(05 Mar 2000)
chondrodystrophy A disturbance in the development of cartilage, primarily the long bones. This can result in arrested growth and dwarfism.
(27 Sep 1997)
chondroectodermal Relating to ectodermally derived cartilage; e.g., branchial cartilages that may have developed from the neural crest.
(05 Mar 2000)
chondroectodermal dysplasia Triad of chondrodysplasia, ectodermal dysplasia, and polydactyly, with congenital heart defects in over half of patients; autosomal recessive inheritance.
Synonym: Ellis-van Creveld syndrome.
(05 Mar 2000)
chondrofibroma <radiology> Benign metaphyseal lesion, young adults (60% less than 30 years of age), lytic lesion with well-defined margin, diaphysis of long bone, proximal TIBIA (especially tubercle) most common, NO calcification Differential diagnosis: bubbly bone lesions
(12 Dec 1998)
chondrogenesis Formation of cartilage.
Synonym: chondrosis.
Origin: chondro-+ G. Genesis, origin
(05 Mar 2000)
chondroglossus See: chondroglossus muscle.
Origin: chondro-+ G. Glossa, tongue
(05 Mar 2000)
chondroglossus muscle <anatomy> Muscular fibres from lesser horn of hyoid bone occasionally separated from the hyoglossus, but usually forming part of it.
Synonym: musculus chondroglossus, ceratoglossus, keratoglossus.
(05 Mar 2000)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 2
  • Chondrodysplasia Punctata, Rhizomelic - »õâ An autosomal recessive form of CHONDRODYSPLASIA PUNCTATA characterized by defective plasmalogen biosynthesis and impaired peroxisomes. Patients have shortened proximal limbs and severely disturbed endochondral bone formation. The metabolic defects associated with the impaired peroxisomes are present only in the rhizomelic form of chondrodysplasia punctata. (From Scriver et al, Metabolic Basis of Inherited Disease, 6th ed, p1497)
    Synonyms : Punctata, Rhizomelic Chondrodysplasia
  • Chondrogenesis - »õâ The formation of cartilage. This process is directed by CHONDROCYTES which continually divide and lay down matrix during development. It is sometimes a precursor to OSTEOGENESIS.
    Synonyms :
  • Chondroitin - »õâ A mucopolysaccharide constituent of chondrin. (Grant & Hackh's Chemical Dictionary, 5th ed)
    Synonyms :
  • Chondroitin ABC Lyase - »õâ An enzyme that catalyzes the eliminative degradation of polysaccharides containing 1,4-beta-D-hexosaminyl and 1,3-beta-D-glucuronosyl or 1,3-alpha-L-iduronosyl linkages to disaccharides containing 4-deoxy-beta-D-gluc-4-enuronosyl groups. (Enzyme Nomenclature, 1992) EC 4.2.2.4.
    Synonyms : Lyase, Chondroitin ABC
  • Chondroitin Lyases - »õâ Enzymes which catalyze the elimination of delta-4,5-D-glucuronate residues from polysaccharides containing 1,4-beta-hexosaminyl and 1,3-beta-D-glucuronosyl or 1,3-alpha-L-iduronosyl linkages thereby bringing about depolymerization. EC 4.2.2.4 acts on chondroitin sulfate A and C as well as on dermatan sulfate and slowly on hyaluronate. EC 4.2.2.5 acts on chondroitin sulfate A and C.
    Synonyms : Chondroitinase-AC II, Chondroitinase AC II, Eliminase, Chondroitin, Lyase, Chondroitin AC, Lyase, Chondroitin B, Lyase, Chondroitin Sulfate, Lyases, Chondroitin, Sulfate Lyase, Chondroitin
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chondrocranium the cartilaginous brain case in bony fishes around which covering bones are laid down
Ãâó: gmbis.marinebiodiversity.ca/BayOfFundy/glossF.html
chondrocalcinosis deposits of calcium crystals in soft tissues; calcification of cartilage.
Ãâó: www.arc.org.uk/about_arth/glossary.htm
chondrocalcinosis Calcification of articular cartilage. May be associated with attacks of joint inflammation that may mimic gout ('Pseudogout').
Ãâó: www.ilar.org/Glossary/Glossary_c.htm
chondrodysplasia Congenital condition in which there is a mutation of a collagen-associated gene.
Ãâó: www.ilar.org/Glossary/Glossary_c.htm
chondrocyte Cartilage cell. Chondrocytes make the structural components of cartilage.
Ãâó: goldbamboo.com/glossary-1c-v1-u-all1.html
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