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  • noun

Synonyms for syndactyly

birth defect in which there is partial or total webbing connecting two or more fingers or toes

References in periodicals archive ?
It was, however, the combination of the 3-4 syndactyly in a growth-restricted infant with a neural tube defect that prompted the consideration of triploidy as the diagnosis.
The main difference from Cruzon syndrome is that it is accompanied by syndactyly of hands and feet.
She also had partial syndactyly of second and third toes, left sided ectropion, reduced intervertebral disc spaces and a spondylolisthesis at lumbosacral level.
In digits, syndactyly and degenerated claws were found and clubbed feet.
On musculoskeletal survey, b/l knee contractures were noted along with b/l ankle ramus deformity, syndactyly was noted in the right foot, marked talipes equinovarus deformity was noted in both the ankles (Figure 1 and 2).
An X-linked inheritance pattern, rib malformations, nail hypoplasia, syndactyly of the second and third fingers and supernumerary nipples are indicative of a diagnosis of SGBS rather than BWS.
There was syndactyly between digits III and IV of both feet.
Ca,L] channels and is accompanied not only by QT prolongation and arrhythmias (LQT syndrome type 8) but also by a wide range of disorders, congenital heart disorders and syndactyly and autism and backwardness and high risk of sudden death at an early age [28].
Syndactyly is a congenital malformation in which two or more fingers are joined because they fail to separate or fuse during limb development.
His brother Archie was born with syndactyly - conjoined fingers where his little finger and ring finger on his right hand fused together.
Being in super- specialty he faced initial resistance from general surgeons, ENT surgeons and orthopaedic surgeons in getting cases of cleft lip, cleft palate, syndactyly and tendon injuries.
These include: supernumerary teeth, hypodontia, pegshaped permanent maxillary lateral incisors, dens in dente, nail disorders, syndactyly, successional conical, macrodontia and double permanent teeth.
Affected individuals of split hand/foot malformation type 1 show absence of central digital rays, deep median clefts, and syndactyly of the digits.
The Poland's Syndrome (also Poland syndrome Poland's syndactyly Poland sequence and Poland's anomaly) (PS) was first described in 1841 by Sir Alfred Poland.