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Klinefelter syndrome is a common condition that results when a person assigned male at birth has an extra copy of the x sex chromosome instead of the typical xy. The clinical features were first described in males with tall stature, small testes, gynecomastia, and azoospermia. Klinefelter syndrome (ks), also known as 47,xxy, is a chromosome anomaly where a male has an extra x chromosome
[10] the complications commonly include infertility and small, poorly functioning testicles (if present). Klinefelter syndrome is a genetic condition characterized by the presence of 2 or more x chromosomes in a phenotypic male Klinefelter syndrome is a common genetic condition in which males have an additional x chromosome
Symptoms may include breast growth, infertility, osteoporosis and learning difficulties.
Most men are born with a pair of xy chromosomes, while most females are born with pair of xx chromosomes Klinefelter syndrome occurs when a male is born with an extra x chromosome Thus a male with klinefelter has xxy instead of the usual xy pair. Klinefelter syndrome, also known as xxy syndrome, is a condition in boys and men that’s caused by an extra x chromosome
It can affect physical and mental development. Recognition and treatment of klinefelter syndrome is important for prevention or treatment of its consequences, such as micropenis, learning disabilities, delayed puberty, infertility, and osteoporosis. Klinefelter syndrome is a genetic condition that affects only males Here's what you should know about the causes, symptoms, and treatment options for the condition.
Klinefelter syndrome is a genetic condition resulting from the presence of one or more extra x chromosomes in males, leading to various physical and psychological issues.
Klinefelter syndrome is a genetic condition that causes an extra x chromosome in people assigned male at birth Also known as xxy syndrome, around one person in every 600 is born with this condition.
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