syndrome Archives - Wellitopia

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...

Klinefelter syndrome is a genetic disorder and is usually seen in male individuals. This syndrome is characterized by one or both of the individual's sex chromosomes having a different structure than normal. Deviation of genetic material from normal results in a variety of effects, from physical characteristics to language and learning abilities. In this article, we will examine this syndrome in detail. What is Klinefelter Syndrome? Klinefelter syndrome is a genetic condition that usually occurs in men. In this syndrome, one or both of the individual's sex chromosomes have a different structure than normal. XXY Chromosome Structure: Genetic Anomaly Individuals with this syndrome usually have an XXY chromosome structure instead of an XY sex chromosome. This condition is associa...

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