Disease & disorder

partial duplication of the long arm of chromosome X

MONDO:0017010

Chromosome Xq duplication is a chromosome abnormality that affects many different parts of the body. People with this condition have an extra copy of the genetic material located on the long arm (q) of the X chromosome in each cell. The severity of the condition and the associated signs and symptoms vary based on the size and location of theduplication;the genes involved; and the sex of the affected person. In general, males are typically more severely affected than females and often experience intellectual disability, developmental delay, short stature, abnormalities of the reproductive organs, anddistinctive craniofacial features. Many females with this duplication do not have any symptoms or are only affected with short stature; however, some may be just as severely affected as males with the condition. Most cases are inherited in an X-linked manner, often from a mother with no signs or symptoms of the condition. Treatment is based on the signs and symptoms present in each person.

Outbreak surveillance

Global reported events

Explore recent public health notices potentially related to partial duplication of the long arm of chromosome X. Results are keyword matches, not yet verified disease-to-outbreak relationships.

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Clinical trials0
Recruiting0
Drug concepts studied0
Synonyms10
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Background context

partial duplication of the long arm of chromosome X

Background only. Canonical identity remains MONDO; clinical-trial relationships come from ClinicalTrials.gov.

Drugs being studied

Disease identity and terminology: MONDO. Trial relationships: ClinicalTrials.gov.