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Tag: turner syndrome chromosome number

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...
Cri-du-chat Syndrome: Deletion in Chromosome 5 and Its Features

Cri-du-chat Syndrome: Deletion in Chromosome 5 and Its Features

Special Psychology
Cri-du-chat syndrome is a genetic disorder that occurs on chromosome 5. In this article, the basic features of the syndrome and the effects of the deletion in chromosome 5 will be discussed. What is Cri-du-chat Syndrome? Cri-du-chat syndrome occurs especially in infancy. It is a genetic condition that involves a number of physical and mental characteristics. This syndrome occurs as a result of the deficiency or deletion of a gene located on chromosome 5. The Effects of Deletion in Chromosome 5: In Cri-du-chat syndrome, the loss of a specific region on chromosome 5 affects the development of the individual. This syndrome is typically recognized by a characteristic feature in which the baby's cry resembles a sound like a cat's meow. In addition, individuals may experience a numb...
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...