Английская Википедия:3p deletion syndrome

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Шаблон:Short description 3p deletion syndrome is a rare genetic disorder caused by the deletion of small fragments of chromosome 3.[1]

Presentation

Reports symptoms in patients with 3p deletion syndrome are intellectual disability, delayed psychomotor development, abnormal facial features, muscular hypotonia, epilepsy, and deformation of the gastrointestinal and urinary tracts.[2]

Clinical phenotypes are often considerably mild, and genetic testing is required for diagnosis.

References

Шаблон:Reflist

Шаблон:Genetic-disorder-stub