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Sex chromosome anomalies belong to a group of genetic conditions that are caused or affected by the loss, damage or addition of one or both sex chromosomes (also called gonosomes). The most frequent scas include turner syndrome (45,x), klinefelter syndrome (47,xxy), trisomy x syndrome (47,xxx), and. Sex chromosome abnormalities may be caused by full or partial deletions or duplications of sex chromosomes
Chromosomes are structures within cells that contain dna and many genes Sex chromosome abnormalities (scas) are chromosomal disorders with either a complete or partial loss or gain of sex chromosomes Genes are segments of deoxyribonucleic acid (dna) and contain the code for a specific protein that functions in one or more types of cells in the body.
Sex chromosome abnormalities may involve aneuploidy, partial deletions or duplications of sex chromosomes, or mosaicism
(see also overview of chromosomal abnormalities.) sex chromosome abnormalities are common genetic conditions characterized by an atypical number or structure of x and/or y chromosomes. Disorders of sexual development (dsds) disorders of sexual development are conditions where a person’s reproductive organs and genitals are “mismatched” at birth Examples include male chromosomes (xy) and genitalia that appears female (vulva) or female chromosomes (xx) and genitalia that appears male (penis) Some people with dsds have characteristics of both sexes.
Sex chromosome abnormalities are genetic conditions caused by atypical numbers or structures of sex chromosomes, affecting development and function.
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