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15q 26.2 Deletion Details

Expanded Description

15q 26.2 Deletion is a rare chromosomal disorder that is characterized by a microdeletion on part of the long arm of chromosome 15.

Prevalence

No prevalence information has been added yet.

Causes

No causes have been added yet.

Disorder Symptoms

Developmental delays (global).
Short stature.
Growth Restriction in utero
Congenital heart disease

We don't have any symptoms yet.

Diagnosis

No diagnosis information has been added yet.

Diagnostic Tests

Deletion so small that it cannot be detected in normal blood test.

We don't have any tests yet.

Disorder Treatments

None known.

We don't have any treatments yet.

Prognosis

Unknown.

Tips for Living with the Disorder

We don't have any tips yet.