多合指症
- 関
- syndactyly
WordNet
- birth defect in which there is partial or total webbing connecting two or more fingers or toes (同)syndactylism
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2015/09/13 16:13:32」(JST)
[Wiki en表示]
Polysyndactyly is an hereditary anatomical malformation combining polydactyly and syndactyly.[1]
References
- ^ http://medical-dictionary.thefreedictionary.com/polysyndactyly
External links
- Polysyndactyly and Marfan's syndrome The case of a family with 17 affected members. The mother also had Marfan's syndrome, which she passed on to a daughter who did not have polysyndactyly.
English Journal
- Comparative study of 2 commissural dorsal flap techniques for the treatment of congenital syndactyly.
- Mallet C, Ilharreborde B, Jehanno P, Litzelmann E, Valenti P, Mazda K, Penneçot GF, Fitoussi F.SourceDepartment of Pediatric Orthopedics, Robert Debré Hospital, Paris, France.
- Journal of pediatric orthopedics.J Pediatr Orthop.2013 Mar;33(2):197-204. doi: 10.1097/BPO.0b013e31827e8ce2.
- BACKGROUND: : Many commissural reconstruction techniques have been described for the treatment of syndactyly. This study is the first to compare long-term results of 2 commissural dorsal flap procedures (T-flap and omega-flap).METHODS: : Fifty-nine web-spaces in 39 patients, operated on between 1991
- PMID 23389576
- A novel phenotype characterized by digital abnormalities, intellectual disability, and short stature in a Mexican family maps to Xp11.4-p11.21.
- Barboza-Cerda MC, Campos-Acevedo LD, Rangel R, Martínez-de-Villarreal LE, Déctor MA.SourceDepartamento de Genética, Facultad de Medicina y Hospital Universitario "José E. González", Universidad Autónoma de Nuevo León, Monterrey, Nuevo León, México.
- American journal of medical genetics. Part A.Am J Med Genet A.2013 Feb;161(2):237-43. doi: 10.1002/ajmg.a.35743. Epub 2013 Jan 10.
- The family observed in this study included affected males and asymptomatic females. The patients shared specific digital abnormalities including postaxial polydactyly, cutaneous syndactyly, and brachydactyly. In addition, the patients exhibited mild-to-moderate intellectual disability and short stat
- PMID 23307567
- Novel SOST gene mutation in a sclerosteosis patient and her parents.
- Bhadada SK, Rastogi A, Steenackers E, Boudin E, Arya A, Dhiman V, Bhansali A, Van Hul W.SourceDept. of Endocrinology and Metabolism, PGIMER, Chandigarh-160012, India. bhadadask@rediffmail.com
- Bone.Bone.2013 Feb;52(2):707-10. doi: 10.1016/j.bone.2012.10.009. Epub 2012 Oct 16.
- INTRODUCTION: Sclerosteosis (OMIM 269500) is a rare autosomal recessive condition characterized by increased bone density associated with syndactyly. It is linked to a genetic defect in the SOST gene coding for sclerostin. So far, six different loss-of-function mutations in SOST have been reported i
- PMID 23079137
Japanese Journal
- 多趾,多合趾症 (特集 手足の先天異常はこう治療する)
- 外側趾列多合趾症手術における作図の工夫 : より自然な外観と余剰皮膚の有効利用
- 専門医取得に必要な形成外科手技 : 口頭試問への対策(6)小趾列多合趾症
Related Links
- Polysyndactyly definition at Dictionary.com, a free online dictionary with pronunciation, synonyms and translation. Look it up now! Added to Favorites Dictionary Thesaurus Word Dynamo Quotes Reference Translator Spanish n. ...
- polysyndactyly /poly·syn·dac·ty·ly/ (-sin-dak´tĭ-le) an association of polydactyly and syndactyly of varying degrees of both the hand and foot. pol·y·syn·dac·ty·ly (p l-s n-d k t-l) n. A congenital condition in which multiple fingers or toes ...
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- 英
- polysyndactyly
- 関
- 合指症