Skip to search formSkip to main contentSkip to account menu

Foot polydactyly

Known as: Duplication of bones of the toes, extra toe, Polydactyly of toes 
A kind of polydactyly characterized by the presence of a supernumerary toe or toes. [HPO:probinson]
National Institutes of Health

Related topics

Related topics

2 relations

Broader (1)

Polydactyly
accessory organ

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2010
Review
2010
Birth defects caused by mutations in human GLI3 and mouse Gli3 genes
GLI3 is the gene responsible for Greig cephalopolysyndactyly syndrome (GCPS), Pallister–Hall syndrome (PHS) and Postaxial… 
Highly Cited
1999
Highly Cited
1999
Mouse Dac, a novel nuclear factor with homology to Drosophila dachshund shows a dynamic expression in the neural crest, the eye, the neocortex, and the limb bud
Dac is a novel nuclear factor in mouse and humans that shares homology with Drosophila dachshund (dac). Alignment with available… 
1997
1997
Polydactyly of the foot: manifestations and treatment.
Polydactyly of the foot is not an uncommon foot problem. However, it is not well understood and not often reported. Its clinical… 
1992
1992
Preaxial polydactyly of feet in infants of diabetic mothers: epidemiological test of a clinical hypothesis.
Using data from the Spanish Collaborative Study of Congenital Malformations (ECEMC), we tested the hypothesis of Carey et al… 
1990
1990
Lambotte syndrome: microcephaly, holoprosencephaly, intrauterine growth retardation, facial anomalies, and early lethality--a new sublethal multiple congenital anomaly/mental retardation syndrome in…
We report on an Arabic sibship originating from Morocco in which four children manifest an undiagnosed sublethal multiple… 
Highly Cited
1988
Highly Cited
1988
Greig cephalopolysyndactyly syndrome: a possible mouse homologue (Xt-extra toes).
Greig cephalopolysyndactyly syndrome is an autosomal dominant form of complex polydactyly in man. Attention is called to the… 
1987
1987
Evidence for negative control of growth by adenosine in the mammalian embryo: induction of Hmx/+ mutant limb outgrowth by adenosine deaminase.
We investigated the growth-regulatory actions of adenosine and adenosine deaminase (ADA) during embryonic limb development in the… 
1986
1986
The murine gamma-chain of the T cell receptor is closely linked to a spermatocyte specific histone gene and the beige coat color locus on chromosome 13.
With the use of standard genetic techniques, we have mapped the T cell gamma-chain gene locus (Tcrg) to the proximal end of mouse… 
Review
1985
Review
1985
The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature.
The Greig cephalopolysyndactyly syndrome in characterized by a set of craniofacial defects (macrocephaly, broad nasal root… 
1971
1971
Bilateral aplasia of the tibia, polydactyly and absent thumb in father and daughter.
1. A family is reported in which tibial aplasia with polydactyly of hands and feet and absent thumbs occurred in a father and… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)