Related Experiment Video
Updated: Jul 10, 2025

09:26
Quantification of Orofacial Phenotypes in Xenopus
Published on: November 6, 2014
9.8K
[Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome]
Krisztina Bartalis1, Bernadette Kálmán2,3, Mihály Kisely1
11 Vas Vármegyei Markusovszky Egyetemi Oktatókórház, Fül-Orr-Gégészeti és Fej-Nyaksebészeti Osztály Szombathely, Markusovszky u. 5., 9700 Magyarország.
Orvosi Hetilap
|November 19, 2023
Summary
Ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC) is a rare genetic disorder. Whole exome sequencing identified a TP63 gene mutation in a sporadic case, enabling genetic counseling and prenatal diagnostics.
Area of Science:
- Genetics
- Rare Diseases
- Developmental Biology
Background:
- Ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC) is a rare autosomal dominant disorder.
- Characterized by ectrodactyly, ectodermal dysplasia, and cleft lip/palate, with variable organ involvement.
- Sporadic cases present diagnostic and management challenges.
Related Concept Videos
Desmosomes
5.4K
The term desmosome derives from the Greek words "desmo" and "soma" meaning "adhesion bodies." This structure was first observed during the late 1800s and described as small, dense nodules in the epidermis. Desmosomes are button-like structures that help form an interlinked network of intermediate filaments across the cells. These junctions are essential to hold cells together under mechanical stress and to maintain tissue integrity. Desmosomes are multi-protein...
5.4K
Nondisjunction
3.9K
Nondisjunction is the failure of homologous chromosomes or sister chromatids to separate correctly and move to the opposite poles of the cells. This produces daughter cells with abnormal chromosome numbers. Nondisjunction is common during anaphase I or anaphase II of meiosis. Mutations in synaptonemal complex proteins that attach homologous chromosomes increase the chances of nondisjunction in anaphase I of meiosis I. In contrast, mutations in topoisomerases and condensins that hold...
3.9K
Pleiotropy
40.5K
Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
40.5K
Cohesins
4.5K
Cohesin protein complexes are a molecular glue that holds two sister chromatids together. They play an important role both in mitosis and meiosis. In mitosis, all cohesin complexes present on the chromosomes are removed before the start of the anaphase stage.
Cohesin complexes in Meiotic Division
Meiosis involves two distinct rounds of chromosomal segregation and cell divisions— Meiosis I followed by Meiosis II – producing four daughter cells. Meiosis I includes the separation of...
Cohesin complexes in Meiotic Division
Meiosis involves two distinct rounds of chromosomal segregation and cell divisions— Meiosis I followed by Meiosis II – producing four daughter cells. Meiosis I includes the separation of...
4.5K
Meiosis I
193.7K
Meiosis is a carefully orchestrated set of cell divisions, the goal of which—in humans—is to produce haploid sperm or eggs, each containing half the number of chromosomes present in somatic cells elsewhere in the body. Meiosis I is the first such division, and involves several key steps, among them: condensation of replicated chromosomes in diploid cells; the pairing of homologous chromosomes and their exchange of information; and finally, the separation of homologous chromosomes by...
193.7K
Structure of Cadherins
3.4K
The cadherins were one of the first cell adhesion molecules discovered; the term “cadherins” is based on their calcium-dependent adhering properties. The first cadherins discovered on the epithelial, neuronal, and placental cells were named E-cadherin, P-cadherin, and N-cadherin, respectively. These classical cadherins share sequence and structural similarities. Other cadherins, including those involved in cell signaling, are grouped into non-classical cadherins. This...
3.4K

