出典: meddic


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「birth defect characterized by the presence of more than the normal number of fingers or toes」

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出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2013/02/07 00:05:27」(JST)

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  • Mutations in TMEM231 cause Meckel-Gruber syndrome.
  • Shaheen R, Ansari S, Mardawi EA, Alshammari MJ, Alkuraya FS.SourceDevelopmental Genetics Unit, King Faisal Specialist Hospital and Research Center, MBC-03 PO BOX 3354, Riyadh 11211, Saudi Arabia; falkuraya@kfshrc.edu.sa.
  • Journal of medical genetics.J Med Genet.2013 Mar;50(3):160-2. doi: 10.1136/jmedgenet-2012-101431. Epub 2013 Jan 24.
  • BACKGROUND: Meckel-Gruber syndrome (MKS) is a genetically heterogeneous severe ciliopathy characterised by early lethality, occipital encephalocele, polydactyly, and polycystic kidney disease.PURPOSE: To report genetic analysis results in two families in which all known MKS diseases genes have been
  • PMID 23349226
  • Radial polydactyly: proposal for a new classification system based on the 159 duplicated thumbs.
  • Chung MS, Baek GH, Gong HS, Lee HJ, Kim J, Rhee SH.Source*Department of Orthopedic Surgery, Seoul National University College of Medicine †Department of Orthopedic Surgery, Seoul National University Boramae Medical Center, Seoul, Korea.
  • Journal of pediatric orthopedics.J Pediatr Orthop.2013 Mar;33(2):190-6. doi: 10.1097/BPO.0b013e3182648ca8.
  • BACKGROUND: : Polydactyly is one of the most common congenital differences that affect the hand. It has various anatomic and morphologic features. Although the Wassel classification has been used widely for radial polydactyly, it is based on the anatomic level of duplication and has some limitations
  • PMID 23389575
  • Novel homozygous mutations in the genes ARL6 and BBS10 underlying Bardet-Biedl syndrome.
  • Khan S, Ullah I, Irfanullah, Touseef M, Basit S, Khan MN, Ahmad W.SourceDepartment of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University Islamabad, Pakistan.
  • Gene.Gene.2013 Feb 15;515(1):84-8. doi: 10.1016/j.gene.2012.11.023. Epub 2012 Dec 6.
  • Bardet-Biedl syndrome (BBS) is an autosomal recessive disorder resulting from structural and functional defects in numerous organs. Frequent manifestations reported in the syndrome include obesity, renal dysplasia, cognitive impairment, postaxial polydactyly, pigmentary retinal degeneration and hypo
  • PMID 23219996


  • 専門医取得に必要な形成外科手技 : 口頭試問への対策(4)母指多指症
  • 症例 特異な形態を呈した小指多指症の1例
  • 土井 悠人,島田 賢一,置塩 良政
  • 形成外科 54(2), 201-205, 2011-02-00
  • NAID 40018712642
  • Double triangular dorsal sliding flap を用いた中手骨型母指多指症の治療
  • 岡本 正則,松田 智,加藤 博之
  • 日本手外科学会雑誌 = The journal of Japanese Society for Surgery of the Hand 26(5), 438-440, 2010-09-13
  • NAID 10026722736


Having extra fingers or toes (6 or more) can occur on its own. There may not be any other symptoms or disease present. Polydactyly may be passed down in families. This trait involves only one gene that can cause ...
:the condition of having more than the normal number of toes or fingers—called also polydactylia, polydactylism ... Seen and Heard What made you want to look up polydactyly? Please tell us where you read or heard it (including the ...






polydactyly, polydactylism
指趾過剰症 supernumerary fingers supernumerary toes



WordNet   license wordnet

「of or relating to a person (or other vertebrate) having more than the normal number of digits」