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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
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on
"https://www.orphadata.com"
. Data version 1.3.16 / 4.1.7.