camptomelic

camptomelic
Denoting or characteristic of camptomelia. See c. syndrome.

Medical dictionary. 2011.

Игры ⚽ Поможем написать курсовую

Look at other dictionaries:

  • camptomelic dwarfism — dwarfism due to camptomelia of the lower limbs, often accompanied by cleft palate, retrognathia, and other abnormalities. Camptomelic dwarfism, showing deformities of the distal long bones …   Medical dictionary

  • camptomelic syndrome — osteochondrodysplasia associated with flat facies, bowed tibiae with skin dimpling, hypoplastic scapulae, and short vertebrae …   Medical dictionary

  • CMD — camptomelic dwarfism; camptomelic dysplasia; cartilage matrix deficiency; cerebromacular degeneration; Certified Medical Densitometrist; chief medical director; childhood muscular dystrophy; common mental disorder; comparative mean dose;… …   Medical dictionary

  • CMD — • camptomelic dwarfism; • camptomelic dysplasia; • cartilage matrix deficiency; • cerebromacular degeneration; • Certified Medical Densitometrist; • chief medical director; • childhood muscular dystrophy; • common mental disorder; • comparative… …   Dictionary of medical acronyms & abbreviations

  • Campomelic dysplasia — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 33419 ICD10 = ICD9 = ICDO = OMIM = 114290 MedlinePlus = eMedicineSubj = eMedicineTopic = eMedicine mult = MeshID = Camptomelic dysplasia is a genetic disorder, camptomelic or campomelic refer …   Wikipedia

  • camptomelia — A skeletal dysplasia characterized by a bending of the long bones of the extremities, resulting in a permanent bowing or curvature of the affected part. [G. kamptos, bent, + melos, limb] * * * camp·to·me·lia (kamp″to meґle ə) [campto + …   Medical dictionary

  • List of diseases (C) — A list of diseases in the English wikipedia.C* C syndrome * C1 esterase deficiency (angioedema)CaCac Cal* Cacchi Ricci disease * CACH syndrome * Cafe au lait spots syndrome * Caffey disease * CAHMR syndrome * Calcinosis cutis (see also CREST… …   Wikipedia

  • Chromosome 17 (human) — Chromosome 17 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 17 spans more than 81 million base pairs (the building material of DNA) and represents between 2.5 and 3 % of the… …   Wikipedia

  • Dwarfism — Abnormally short stature, which may be due to a variety of causes. Some forms are hereditary. See also {{}}achondroplasia; dwarfism, pituitary. * * * A condition or a group of conditions in which the standing height of the person is below the 3rd …   Medical dictionary

  • osteochondrodysplasia — SYN: camptomelic syndrome. * * * os·teo·chon·dro·dys·pla·sia .kän drō .dis plā zh(ē )ə n abnormal growth or development of cartilage and bone * * * os·teo·chon·dro·dys·pla·sia (os″te o kon″dro dis plaґzhə) [osteo + chondro + dys… …   Medical dictionary

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”