- limb malformation
- уродство конечности
English-Russian small dictionary of medicine. Г.Ю. Бельман, А.Е. Бойков.. 2015.
limb malformation
Смотреть что такое "limb malformation" в других словарях:
Limb-girdle muscular dystrophy — Classification and external resources ICD 10 G71.0 ICD 9 359.1 … Wikipedia
malformation — /mal fawr may sheuhn, feuhr /, n. faulty or anomalous formation or structure, esp. in a living body: malformation of the teeth. [1790 1800; MAL + FORMATION] * * * ▪ biology Introduction in biology, irregular or abnormal structural… … Universalium
Malformation, congenital — A physical defect present in a baby at birth, irrespective of whether the defect is caused by a genetic factor or by prenatal events that are not genetic. In a malformation, the development of a structure is arrested, delayed, or misdirected… … Medical dictionary
Split-hand/split-foot malformation — A genetic malformation syndrome of the limbs with syndactyly, median clefts of the hands and feet, and aplasia (failure of development) and/or hypoplasia (underdevelopment) of the phalanges (the digits), the metacarpals (the bones leading up to… … Medical dictionary
Congenital malformation — A physical defect present in a baby at birth, irrespective of whether the defect is caused by a genetic factor or by prenatal events that are not genetic. In a malformation, the development of a structure is arrested, delayed, or misdirected… … Medical dictionary
Ectrodactyly-ectodermal dysplasia-cleft syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 34402 ICD10 = ICD9 = ICDO = OMIM = 129900 OMIM mult = OMIM2|604292 | MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Ectrodactyly ectodermal dysplasia cleft syndrome, or EEC, is a… … Wikipedia
HOXD13 — Homeobox D13, also known as HOXD13, is a human gene.cite web | title = Entrez Gene: HOXD13 homeobox D13| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=3239| accessdate = ] This gene belongs to the homeobox … Wikipedia
Rapadilino syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 34465 ICD10 = ICD9 = ICDO = OMIM = 266280 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Rapadilino syndrome is an autosomal recessivecite journal |author=Kaariainen H, Ryoppy S,… … Wikipedia
thalidomide — A hypnotic drug which, if taken in early pregnancy, may cause the birth of infants with phocomelia and other defects; under investigational use for treatment of leprosy and as an immunomodulator in HIV infections and graft vs. host reactions. * * … Medical dictionary
Holt-Oram syndrome — autosomal dominant heart disease of varying severity, usually an atrial or ventricular septal defect, in association with upper limb malformation consisting of narrow shoulders, hypoplasia of the radius, and phocomelia, most commonly absence of… … Medical dictionary
thalidomide — n. a drug that was formerly used as a sedative. If taken during the first three months of pregnancy, it was found to cause fetal abnormalities involving limb malformation and was withdrawn as a sedative in 1962. Recently, however, thalidomide has … The new mediacal dictionary
