نتایج جستجو برای: symmetric syndactyly

تعداد نتایج: 81613  

مجتهدزاده , فریدون, نخشب , مریم, پورفاطمی , فاطمه,

Âpert syndrome is a case syndrome with an incidence of about 16 in 1,000,000 live births. Ït is classified with the Âcrocephalosyndactyly syndromes, which is cranyosynostosis in combination with syndactyly in hands and feet. The other common clinical manifestations in Âpert Syndrome are acrocephaly, Turibrachycephaly, syndactyly on hands and feet, wide Tumb, ante mongoloid polpebral fissure, ...

2015
Hao Deng Ting Tan

Syndactyly, webbing of adjacent digits with or without bony fusion, is one of the most common hereditary limb malformations. It occurs either as an isolated abnormality or as a component of more than 300 syndromic anomalies. There are currently nine types of phenotypically diverse nonsyndromic syndactyly. Non-syndromic syndactyly is usually inherited as an autosomal dominant trait, although the...

Journal: :Journal of the College of Physicians and Surgeons Pakistan 2019

Journal: :Journal of medical genetics 1990
L A Brueton S M Huson B Farren R M Winter

A family is described with type III syndactyly and facies resembling the oculodentodigital dysplasia facial phenotype in the absence of any of the other characteristic findings of the latter condition. The relationship between type III syndactyly and oculodentodigital dysplasia is discussed.

Journal: :Revista do Hospital das Clinicas 1999
P Tuma G Arrunategui A Wada H Friedhofer M C Ferreira

The authors analysed a series of 22 patients undergoing surgical correction of congenital hand syndactyly by the rectangular flap technique. Using our evaluation method, we found that good functional and aesthetic results were obtained in 77.3% of the patients, with a complication rate of 13.6%. We concluded that the rectangular flap technique has a simple design, is easily reproducible by in-t...

Journal: :Proceedings of the Royal Society of Medicine 1923

Journal: :Journal of medical genetics 1986
P Merlob M Grunebaum

A new family with syndactyly type II or synpolydactyly is described with 16 affected members in six generations. No other major skeletal or extraskeletal malformations were present, but the association with minor local anomalies may be a common feature. Various metacarpal or metatarsal abnormalities may be part of this type of syndactyly. The family pedigree confirms the autosomal dominant mode...

Journal: :Archives of Iranian medicine 2006
Sadralah Motamed Parviz Mafi Mohammad Shariati Ehsan Arasteh

Tissue expanders can be used over the dorsum of hand and fingers to increase available tissue for flap coverage after release of syndactyly. Herein, we presented an 18-year-old man who had an unusual complex syndactyly in the middle and ring fingers of his right hand. He had also complete fusion of the proximal phalanges. In this report, we described the application of tissue expander to cover ...

2013
Meera Sandhu Pooja Malik Rooposhi Saha

Filippi syndrome is an autosomal recessive condition characterized by variable soft tissue syndactyly of the fingers and toes, microcephaly, pre- and postnatal growth retardation, mildly abnormal craniofacial appearance, and mental retardation. We report on a child with Filippi syndrome who shows syndactyly of fingers, severe postnatal growth retardation, postnatal microcephaly, and moderate to...

Journal: :Archives of Hand and Microsurgery 2022

Harlequin ichthyosis (HI) is a rare congenital disease that primarily affects the skin. Its complications include syndactyly, which can cause severe constriction. Surgical release thought to be helpful, but details remain unclear due lack of data. We share our 5-year experience patient with HI successful outcomes from five syndactyly operations involving division, local flap interposition, and ...

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