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birth defect in which there is partial or total webbing connecting two or more fingers or toes (同)syndactylism

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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)

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

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