- osseous syndactyly
- костная синдактилия
English-Russian dictionary of medicine. Г.Ю. Бельман, А.Е. Бойков. 2015.
English-Russian dictionary of medicine. Г.Ю. Бельман, А.Е. Бойков. 2015.
Synostosis — Osseous union between the bones forming a joint, an example being the paired frontal bones of the skull which normally fuse along the metopic suture postnatally.In medical contexts, synostosis is the abnormal development of a joint. It is a type… … Wikipedia
syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… … 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
List of diseases (B) — A listing of diseases in the English wikipedia.DiseasesTOC BaBab Bam* Baber s syndrome * Babesiosis * Bacterial endocarditis * Bacterial food poisoning * Bacterial gastroenteritis * Bacterial meningitis * Bacterial pneumonia * Bacterial vaginalis … Wikipedia
Dysplasia — Abnormal in form. From the Greek dys (bad, disordered, abnormal) and plassein (to form). For example, retinal dysplasia is abnormal formation of the retina during embryonic development. * * * Abnormal tissue development. SEE ALSO: heteroplasia.… … Medical dictionary
Bardet–Biedl syndrome — Laurence Moon Biedl syndrome and Laurence Moon Biedl Bardet redirect here. See below for an explanation. Bardet–Biedl syndrome Classification and external resources ICD 10 Q87.8 ICD 9 … Wikipedia
List of diseases (T) — A list of diseases in the English wikipedia.DiseasesTOC T Tc* T cell immunodeficiency primary * Tabatznik syndrome * Tachycardia * Taeniasis * Takayasu arteritis * Talipes equinovarus * Tamari Goodman syndrome * Tang Hsi Ryu syndrome * Tangier… … Wikipedia
oculodentodigital dysplasia — (ODDD), oculodento osseous dysplasia (ODOD) a rare hereditary condition caused by mutations in the GJA1 gene (locus: 6q21 q23.2), which encodes connexin 43, characterized by bilateral microphthalmos, abnormally small nose with anteverted nostrils … Medical dictionary
Pes cavus — Classification and external resources High arch in foot of a person with a hereditary neuropathy ICD 10 Q … Wikipedia
Larsen syndrome — Classification and external resources OMIM 150250 245600 DiseasesDB 32807 Larsen … Wikipedia