45,X/46,XY mosaicism
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45,X/46,XY mosaicism, also known as X0/XY mosaicism and mixed gonadal dysgenesis,[1] is a mutation of sex development in humans associated with sex chromosome aneuploidy and mosaicism of the Y chromosome. It is a fairly rare chromosomal disorder at birth, with an estimated incidence rate of about 1 in 15,000 live births.[2] Mosaic loss of the Y chromosome in previously non-mosaic men grows increasingly common with age.[3]
45,X/46,XY mosaicism | |
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Other names | 45,X0/46,XY MGD |
Specialty | Obstetrics and gynaecology, endocrinology, medical genetics |
The clinical manifestations are highly variable, ranging from partial virilisation and ambiguous genitalia at birth, to patients with completely male or female gonads. Most individuals with this karyotype have apparently normal male genitalia, and a minority have female genitalia, with a significant number of individuals showing genital abnormalities or intersex characteristics.[4] A significantly higher than average number of other developmental abnormalities are also found in individuals with X0/XY mosaicism.[4] Psychomotor development is normal.