Results 81 to 90 of about 2,276 (204)

Ectrodactyly and Germany's eugenics law of 14 July 1933

open access: yes, 2002
The family reported herein serves as a genetically and historically important vignette on the issues of nonpenetrance (versus germinal mosaicism) in nonsyndromic autosomal dominant ectrodactyly and the Eugenics Law of Germany of 14 July 1933, which was ...
Klaus Kjaer   +3 more
core   +1 more source

ECTRODACTYLY

open access: yes
Citation: 'ectrodactyly' in the IUPAC Compendium of Chemical Terminology, 5th ed.; International Union of Pure and Applied Chemistry; 2025. Online version 5.0.0, 2025. 10.1351/goldbook.10636 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms.
openaire   +2 more sources

Treatment of congenital deformities of cleft foot and syndactyly: A case report and review of the literature

open access: yesTurkish Journal of Plastic Surgery
Cleft foot is a rare congenital anomaly characterized by a central conical defect and deficiency of the foot rays. Syndactyly is the fusion of the skin with or without the bone of adjacent digits, and it may be associated with syndrome-related cleft foot.
Nuh Evin   +3 more
doaj   +1 more source

Ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC): report of a case with perioral papillomatosis

open access: yes, 2002
We report a 13-year-old boy with ectodermal dysplasia, ectrodactyly, and syndactyly, hypospadias, photophobia, conductive hearing loss, and perioral papillomatosis. His father had ectrodactyly and hypotrichosis.
Machado, A   +3 more
core  

Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome Associated With p63 Mutation and an Uncommon Phenotype

open access: yes, 2015
Ectrodactyly-ectodermal dysplasia-clefting syndrome is an uncommon disorder that includes a clinical spectrum of limb, facial, ocular, internal ear, and urogenital malformations.
Abdo, RC   +5 more
core   +1 more source

Table1_Case report: Prenatal diagnosis of Ectrodactyly–Ectodermal dysplasia–Cleft syndrome (EEC) in a fetus with cleft lip and polycystic kidney.docx

open access: yes, 2022
Ectrodactyly–ectodermal dysplasia–cleft (EEC) syndrome is an autosomal dominant disorder characterized by ectrodactyly, ectodermal dysplasia, and orofacial clefting.
Cheng Weiwei (12676577)   +9 more
core   +1 more source

Toes, tails, and heads: Morphological anomalies in different lizard species of Central Mexico

open access: yesActa Herpetologica
Morphological anomalies in reptiles can originate from genetic factors, trauma, infections, or environmental conditions and affect key aspects such as locomotion, behavior, and survival. Here, we document 24 cases of morphological anomalies in the toes,
Alexis M. Leonardo-González   +9 more
doaj   +1 more source

Characterization of two ectrodactyly-associated translocation breakpoints separated by 2.5 Mb on chromosome 2q14.1-q14.2.

open access: yes, 2009
Contains fulltext : 80019.pdf (Publisher’s version ) (Open Access)Split hand-split foot malformation or ectrodactyly is a heterogeneous congenital defect of digit formation.
Paula Vieira   +20 more
core   +1 more source

EEC syndrome (ectrodactyly-ectodermal dysplasia-clefting): A clinical case report

open access: yes, 2021
The EEC syndrome (ectrodactyly-ectodermal dysphasia-clefting) is defined as a multiple congenital anomaly syndrome characterized by ectodermal dysplasia, distal limb anomaly; cleft lip/palate, and lacri man duct anomalies.
Bilgin, T, Yalcin, S, Ulukapi, I
core  

BMP-mediated functional cooperation between Dlx5;Dlx6 and Msx1;Msx2 during mammalian limb development.

open access: yesPLoS ONE, 2013
The Dlx and Msx homeodomain transcription factors play important roles in the control of limb development. The combined disruption of Msx1 and Msx2, as well as that of Dlx5 and Dlx6, lead to limb patterning defects with anomalies in digit number and ...
Maxence Vieux-Rochas   +13 more
doaj   +1 more source

Home - About - Disclaimer - Privacy