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Xxxy syndrome is a genetic condition characterized by a sex chromosome aneuploidy, where individuals have two extra x chromosomes These conditions share some of the features of xxy such as testicular failure in adolescence and tall stature, however, they are more commonly associated with learning/cognitive disabilities, language. [3] people in most cases have two sex chromosomes
An x and a y or two x chromosomes. There are some other sca conditions such as 48,xxyy, 48,xxxy, and 49,xxxxy that are sometimes also called variants of klinefelter syndrome 48,xxxy syndrome is a chromosomal condition in boys and men that causes intellectual disability, developmental delays, physical differences, and an inability to father biological children (infertility)
Explore symptoms, inheritance, genetics of this condition.
48,xxxy syndrome is a type of chromosome abnormality characterized by the presence of 2 extra x chromosomes in males It is sometimes referred to as a variant of klinefelter syndrome, but differs from klinefelter syndrome in many ways and is usually more severe Signs and symptoms of 48,xxxy syndrome can vary but may include learning difficulties Xxxy syndrome is an abnormal chromosomal condition affects only male individuals
The name of the syndrome indicates extra sex chromosomes is the main clinical presentation of this disorder. Xxxy syndrome xxxy syndrome is a chromosome condition that only affects males It is rare and there is little specific information available Individuals with the condition have a wide spectrum of physical, developmental and behavioural characteristics, ranging from mild to severe
Interventional therapies such as physiotherapy and speech therapy, individual educational plans and ongoing.
The xxxy syndrome is a sex chromosome that affects one in 17,000 boys It can also be called 48, xxxy syndrome because such individual has 48 chromosomes instead of the normal 46, due to the extra two sex chromosomes Most researchers believe that 48, xxxy syndrome is a variation of klinefelter syndrome (xxy syndrome), with the 47, xxy syndrome's dysmorphic features being mild, multiple and. The 48,xxxy syndrome differs from klinefelter syndrome by the presence of moderate intellectual deficit (average iq of 50), more marked genital hypoplasia (microorchidism, micropenis, hypoplasia of the scrotum) and by more frequently observed facial dysmorphism (flat nose, epicanthus, prognathism, short neck, hypertelorism, facial asymmetry)
Other dysmorphic characteristics (clinodactyly of. Xxxy syndrome is a genetic disorder characterized by a sex chromosome aneuploidy, where males have two extra x chromosomes Males typically have only two sex chromosomes, an x and a y. 48, xxxy can result from meiotic or mitotic nondisjunction and is often considered a variant of klinefelter syndrome (47, xxy)
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