- congenital osteogenesis imperfecta
- врожденное несовершенное костеобразование
English-Russian dictionary of medicine. Г.Ю. Бельман, А.Е. Бойков. 2015.
congenital osteogenesis imperfecta
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Osteogenesis imperfecta — Classification and external resources The classic blue sclerae of a person with osteogenesis imperfecta ICD 10 Q … Wikipedia
Osteogenesis imperfecta — Brittle bone disease. Osteogenesis imperfecta (OI) is not one but a group of genetic diseases, all of which affect collagen in connective tissue in the body and all of which result in fragile bones. The best known types are types I and II. * * *… … Medical dictionary
osteogenesis imperfecta — fragilitas ossium a congenital disorder of connective tissue formation that affects bone, teeth, and soft tissues. It has an incidence of 1 in 20,000 and there are four types, of varying severity, the worst being lethal at birth. In all types the … The new mediacal dictionary
Congenital stromal corneal dystrophy — Classification and external resources The cornea is particularly opaque in the anterior stroma by slit lamp biomicroscopy OMIM … Wikipedia
embryotoxon — Congenital opacity of the periphery of the cornea, a feature of osteogenesis imperfecta. [embryo + G. toxon, bow] anterior e. SYN: arcus senilis. posterior e. a common developmental abnormality marked by a prominent white … Medical dictionary
Список наследственных заболеваний — Список генетических заболеваний Основные статьи: наследственные заболевания, Наследственные болезни обмена веществ, Ферментопатия. В большинстве случаев приведен также код, указывающий на тип мутации и связанные с ней хромосомы. См. также система … Википедия
endocrine system, human — ▪ anatomy Introduction group of ductless glands (gland) that regulate body processes by secreting chemical substances called hormones (hormone). Hormones act on nearby tissues or are carried in the bloodstream to act on specific target organs… … Universalium
bone disease — Introduction any of the diseases or injuries that affect human bones (bone). Diseases and injuries of bones are major causes of abnormalities of the human skeletal system (skeletal system, human). Although physical injury, causing fracture,… … Universalium
Chromosome 7 (human) — Chromosome 7 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 7 spans more than 158 million base pairs (the building material of DNA) and represents between 5 and 5.5 percent of the… … Wikipedia
Hommes de verre — Ostéogenèse imparfaite L ostéogenèse imparfaite (du latin osteogenesis imperfecta) est un groupe de maladies caractérisées par une fragilité osseuse excessive, due à un défaut congénital d élaboration des fibres collagènes du tissu conjonctif qui … Wikipédia en Français
Maladie des os de verre — Ostéogenèse imparfaite L ostéogenèse imparfaite (du latin osteogenesis imperfecta) est un groupe de maladies caractérisées par une fragilité osseuse excessive, due à un défaut congénital d élaboration des fibres collagènes du tissu conjonctif qui … Wikipédia en Français
