Microduplication Xp11.22p11.23 syndrome
What is Microduplication Xp11.22p11.23 syndrome?
Familial and de novo recurrent Xp11.22-p11.23 microduplication has been recently identified in males and females.
Other condition names
- Dup(X)(p11.22p11.23)
- Trisomy Xp11.22p11.23
Inheritance type
Not applicable, X-linked dominant
Prevalence
- Worldwide: <1 in 1,000 000
Age of Onset
- Infancy
- Neonatal
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