49 XXXXY syndrome

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49 XXXXY Syndrome is an extremely rare, aneuploidic sex chromosomal abnormality; its frequency is approximately 1 out of 85,000 to 100,000 males.^[1] As its name indicates, a person with the syndrome has one Y chromosome and four X chromosomes on the 23^rd pair, thus having 49 chromosomes rather than the normal 46. As is common with aneuploidy disorders, 49 XXXXY syndrome is often accompanied by mental retardation. It can be considered a variant of Klinefelter syndrome.^[1]

It is genetic, but not hereditary. This means that while the genes of the parents cause the syndrome, there is a small chance of more than one child having the syndrome. The probability of inheriting the disease is about 1%.^[2]

The individuals with this syndrome are males, but a female version also exists with similar characteristics as the male version.

Contents 1 Effects 2 Causes 3 References 4 External links 5 See also

[edit] Effects

Aneuploidy is often fatal, but in this case there is "X-inactivation" where the effect of the extra chromosomes would be reduced and thus made safer by the body.^[2]

The mental effects of 49 XXXXY Syndrome vary, much like Down syndrome. Males with the syndrome tend to have impaired speech and behavioral problems. Those with 49 XXXXY syndrome tend to exhibit infantile secondary sex characteristics with sterility in adulthood and have some skeletal anomalies. Skeletal anomalies include:

• genu valgus
• pes cavus
• fifth finger clinodactyly.

The effects on the males also include:

• cleft palate
• club feet
• respiratory conditions
• short or/and broad neck
• low birth weight
• hyperextensible joints
• short stature
• narrow shoulders
• coarse features in older age
• hypertelorism
• epicanthal folds
• prognathism
• gynecomastia (rare)
• muscular hypotonia
• hypoplastic genitalia
• cryptorchidism
• congenital heart defects
• a very round face in infancy.^[2]

[edit] Causes

49 XXXXY syndrome is caused in males because of a lack of a testosterone surge in utero. They also miss a second testosterone growth shortly after birth, while normal male babies experience both of these.^[2]

[edit] References

[edit] External links

• 49,XXXXY Syndrome.com
• 49 XXXXY at the National Organization of Rare Diseases

[edit] See also

• aneuploidy
• Turner syndrome
• Klinefelter syndrome
• 49, XXXXX, a similar syndrome related to females

v • d • e Pathology: chromosome abnormalities (Q90-Q99, 758) Autosomal trisomies Down syndrome (21), Edwards syndrome (18), Patau syndrome (13), Trisomy 9, Warkany syndrome 2 (8), Cat eye syndrome (22), Trisomy 22, Trisomy 16 Autosomal monosomies/deletions Wolf-Hirschhorn syndrome (4), Cri du chat (5), Williams syndrome (7), Angelman syndrome/Prader-Willi syndrome (15), Miller-Dieker syndrome/Smith-Magenis syndrome (17), 22q11.2 deletion syndrome (22) X/Y linked Monosomy: Turner syndrome (XO) Trisomy: Triple X syndrome (XXX), Klinefelter's syndrome (XXY), XYY Other Karyotypes: XXXX, XXYY, XXXXX, XXXXY Translocations Philadelphia chromosome, Burkitt's lymphoma Other Fragile X syndrome, Gonadal dysgenesis (Mixed gonadal dysgenesis)