chromosome 15q24 deletion syndrome

15q24 microdeletion syndrome is a rare chromosomal anomaly characterized cytogenetically by a 1.7-6.1 Mb deletion in chromosome 15q24 and clinically by pre- and post-natal growth retardation, intellectual disability, distinct facial features, and genital, skeletal, and digital anomalies.

Also known as: 15q24 microdeletion syndrome, 15q24 recurrent microdeletion syndrome, Del(15)(q24), monosomy 15q24, WITKOS

Category: General

What is chromosome 15q24 deletion syndrome?

chromosome 15q24 deletion syndrome is a recognized medical condition. This page explains what it is, symptoms that may accompany it, and the lab tests healthcare providers sometimes use to investigate it. It is educational information only and is not a diagnosis.

If you think you may have chromosome 15q24 deletion syndrome, speak with a qualified healthcare provider for evaluation and guidance.

Symptoms that may be associated with chromosome 15q24 deletion syndrome

AnxietyConstipationDeeply set eyeFatigueGastroesophageal refluxHearing impairmentIntracranial hemorrhageSeizureSensorineural hearing impairment

When to seek medical care

Seek medical advice if you have symptoms that are severe, persistent, or affecting your daily life. Emergency care is needed for symptoms like chest pain, difficulty breathing, confusion, or severe weakness.