48,XXYY Syndrome Details

Expanded Description

48,XXYY syndrome is a rare genetic condition caused by a chromosome aneuploidy.

Prevalence

2.5 ( Per 100,000 Population ) [Source]

Causes

No causes have been added yet.

Disorder Symptoms

No symptom information has been added yet.

We don't have any symptoms yet.

Diagnosis

48 XXYY syndrome is diagnosed either by prenatal testing during pregnancy or by a blood test which examines the chromosomes (karyotype) of the patient.

Diagnostic Tests

No diagnostic test information has been added yet.

We don't have any tests yet.

Disorder Treatments

No treatment information has been added yet

We don't have any treatments yet.

Prognosis

No prognosis information has been added yet

Tips for Living with the Disorder

We don't have any tips yet.