postaxial polydactyly

postaxial polydactyly
постаксиальная полидактилия

English-Russian small dictionary of medicine. . 2015.

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  • Polydactyly — or polydactylism (from Ancient Greek (polus) many + δάκτυλος (daktulos) finger ), also known as hyperdactyly, is a congenital physical anomaly consisting of supernumerary fingers or toes. When each hand or foot has six digits, it is sometimes… …   Wikipedia

  • Polydactyly (hexadactyly) — The presence of an extra, sixth finger or toe, a very common congenital malformation (birth defect). This is called hexadactyly. The word hexadactyly literally means six digits. In medical usage, hexadactyly does not specify whether the six… …   Medical dictionary

  • List of diseases (P) — A list of diseases in the English Wikipedia.DiseasesTOC PaPac Pal* Pachydermoperiostosis * Pachygyria * Pachyonychia congenita Jackson Lawler type * Pacman dysplasia * Paes Whelan Modi syndrome * Paget disease extramammary * Paget disease… …   Wikipedia

  • List of diseases (H) — A list of diseases in the English wikipedia.DiseasesTOC HaHag Ham* Hageman factor deficiency * Hagemoser Weinstein Bresnick syndrome * Hailey Hailey disease * Hair defect with photosensitivity and mental retardation * Hairy cell leukemia * Hairy… …   Wikipedia

  • List of diseases (S) — A list of diseases in the English wikipedia.DiseasesTOC NOTOC Sa Sc Se Sh Si Sj Sn So Sp Sq Ss St Su Sw Sy aSaa Sak Sal Sar Sat Say aa Sal* Saal Bulas syndrome * Saal Greenstein syndrome * Sabinas brittle hair syndrome * Saccharopinuria * Sackey… …   Wikipedia

  • List of diseases (M) — A list of diseases in the English wikipedia.DiseasesTOC MaMac* Mac Ardle disease * Mac Dermot Patton Williams syndrome * Mac Dermot Winter syndromeMaci Macr* Macias Flores Garcia Cruz Rivera syndrome * Mackay Shek Carr syndrome * Macleod Fraser… …   Wikipedia

  • 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

  • GLI3 — GLI Kruppel family member GLI3 (Greig cephalopolysyndactyly syndrome), also known as GLI3, is a human gene.cite web | title = Entrez Gene: GLI3 GLI Kruppel family member GLI3 (Greig cephalopolysyndactyly syndrome)| url =… …   Wikipedia

  • Pallister-Hall syndrome — Classification and external resources OMIM 146510 DiseasesDB 32013 MeSH …   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

  • Androgen insensitivity syndrome — Classification and external resources AIS results when the function of the androgen receptor (AR) is impaired. The AR protein (pictured) mediates the effects of androgens in the human body. ICD 10 E …   Wikipedia


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