Turner’s syndrome is a genetic disorder which mainly affects female growth and development. It is also termed as gonadal dysgenesis which occurs because of the absence of sex chromosome (X). The absence of the X chromosome causes abnormal development in human females. Instead of having a pair of 46 normal XX chromosomes, females with gonadal dysgenesis develop 45,X chromosomes (Castiglia, 1997). This odd combination of chromosomal pairing results in a conflicted sex of the person, where they are neither distinguished as male or female, due to the absence of the second X chromosome that would establish them ...
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Turner syndrome is a typical example of a chromosome abnormality caused by the mutation of the chromosomal DNA complex. It is caused by the missing of one sex chromosome in the body. It is presented when the sexual gene orientation of a lady’s chromosome are not complete and lack some genes (Rosenfeld et al. 23). It is caused during the sexual intercourse when a pair of chromosomes fails to separate hence leading to the formation of an embryo with only one X-chromosome. In the embryo formation during copulation, both the parents give out X-chromosomes leading to XX-chromosomes but ...
Turner’s syndrome is a disease that usually affects females. It occurs when one of the X chromosomes (out of the pair of two XX chromosomes) of a female is either missing completely or partially. It can lead to huge numbers of developmental problems and medical complications. Some of the presenting features are short stature, delayed puberty, infertility, defects in the cardiovascular system, inability to grasp or learn new things and problems with social adjustments. The disease can be diagnosed in the gestational phase of the female or during early years of life. It is a rare occurrence that ...