Saturday, June 29

Tag: chromosomal diseases caused by genetic anomalies

Chromosomal Anomalies and Autism Spectrum Disorder (ASD)

Chromosomal Anomalies and Autism Spectrum Disorder (ASD)

Special Psychology
Chromosomal anomalies and autism spectrum disorder (ASD) are important issues studied in connection with genetic factors. In this article, we will discuss the effects of chromosomal anomalies on Autism Spectrum Disorder (ASD). What are Chromosome Anomalies? Chromosomal anomalies are changes that occur as a result of the irregular distribution of genetic material. Such deviations of genetic information affect the development of the individual. It may contribute to the emergence of neurodevelopmental disorders such as ASD. What is Autism Spectrum Disorder? Autism Spectrum Disorder is a neurodevelopmental disorder characterized by difficulties in social interaction and communication. Genetic components play an important role in brain development and functionality. This may affect...
Effects of Changes in Chromosomes on Human Health

Effects of Changes in Chromosomes on Human Health

Diseases
The human body stores genetic information through chromosomes, one of the basic structural units that carry genetic information. However, changes in these chromosomes can affect an individual's health and cause various genetic diseases. In this article, we will discuss in detail the effects of chromosome abnormalities on human health. From numerical changes such as trisomy and monosomy to structural changes such as deletions and duplications. Changes in Chromosomes and Genetic Structure Human cells contain chromosomes that carry genetic information. Any change in chromosomes affects the genetic structure and causes health problems. Trisomy and Monosomy: Numerical Changes Trisomy refers to the presence of more than normal chromosomes in a chromosome pair. Monosomy represents a ...
Turner Syndrome: Single X Chromosome Anomaly and Its Effects

Turner Syndrome: Single X Chromosome Anomaly and Its Effects

Special Psychology
Turner syndrome is a genetic disorder that usually occurs in girls. This syndrome is characterized by a fundamental abnormality in the individual's genetic makeup: the presence of only one X chromosome. It is a condition that causes significant changes in physical characteristics. It also manifests itself with various effects on growth, sexual development and fertility. In this article, we will examine the basic features and effects of Turner syndrome in detail. What is Turner Syndrome? This syndrome is a genetic disorder usually seen in girls. In this case, the individual is missing one of the sex chromosomes. So there is usually one X chromosome. Single X Chromosome: At the Basis of Genetic Anomalies This syndrome is usually associated with the individual having only one X c...
Chromosomal Diseases Caused by Genetic Anomalies

Chromosomal Diseases Caused by Genetic Anomalies

Diseases
Genetic anomalies cover a range of conditions that refer to abnormalities in the genetic material of individuals. These anomalies usually occur in chromosomes and cause various genetic diseases. Chromosomal diseases occur as a result of changes in the structure or number of genetic material. They can affect individuals' quality of life. In this article, we will examine in detail the mechanisms, symptoms and effects of genetic anomalies, especially those that lead to chromosomal diseases. What are Genetic Anomalies and Chromosomal Diseases? Genetic anomalies refer to abnormalities that occur in the genetic material of individuals. These anomalies usually occur in chromosomes and lead to various chromosomal diseases. Trisomy and Monosomy: Changes in the Number of Chromosomes Tr...