Related Experiment Video
Updated: Sep 1, 2025

08:12
Micro-dissection of Enamel Organ from Mandibular Incisor of Rats Exposed to Environmental Toxicants
Published on: March 29, 2018
10.2K
Ectodermal Dysplasia Presenting as Hypodontia in a Nine-Year-Old Female
Brenda Abreu Molnar1, Alejandro Semidey2, Suzanne Minor3
1Medicine, Florida International University, Herbert Wertheim College of Medicine, Miami, USA.
Cureus
|August 16, 2022
Summary
Ectodermal dysplasia, a disorder affecting ectodermal tissues like teeth, was diagnosed late in an immigrant child due to social factors. Barriers to oral rehabilitation highlight healthcare access challenges.
Area of Science:
- Genetics and Developmental Biology
- Pediatric Dentistry
- Public Health
Background:
- Ectodermal dysplasia (ED) encompasses genetic disorders impacting ectodermal derivatives such as hair, nails, teeth, and glands.
- Abnormal tooth development is a common manifestation of ED, significantly affecting a child's oral health and quality of life.
- Socioeconomic factors and immigration status can create substantial barriers to timely diagnosis and comprehensive treatment for rare genetic conditions.
Keywords:
abnormal teethectodermal dysplasiahypodontiapediatric case reportsocial determinants of health (sdoh)More Related Videos
Related Concept Videos
Teeth
612
The formation of teeth, also known as odontogenesis, is a complex process that begins in utero, around the sixth week of embryonic development. There are three stages to this process: the bud stage, the cap stage, and the bell stage.
In the bud stage, the tooth germ (an aggregation of cells) starts to form in the developing jawbone. During the cap stage, the tooth germ differentiates into enamel organ, dental papilla, and dental sac, which will later develop into the tooth's enamel, dentin...
In the bud stage, the tooth germ (an aggregation of cells) starts to form in the developing jawbone. During the cap stage, the tooth germ differentiates into enamel organ, dental papilla, and dental sac, which will later develop into the tooth's enamel, dentin...
612
Genomic Imprinting and Inheritance
35.1K
Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
35.1K
Nondisjunction
4.0K
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...
4.0K
Oppositional Defiant Disorder
127
A persistent pattern of angry or irritable mood, defiant behavior, or vindictiveness characterizes Oppositional Defiant Disorder (ODD). Symptoms must occur over at least six months, involve interactions with individuals beyond siblings, and meet specific diagnostic criteria to be clinically significant. The disorder affects emotional regulation, social interactions, and behavior, often manifesting early in life and influencing long-term development and functioning.
Diagnostic Criteria and...
Diagnostic Criteria and...
127
Meiosis I
194.2K
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...
194.2K
Teratogenicity
2.6K
The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...
2.6K

