4p16.3 deletion

4p16.3 deletion: Introduction

4p16.3 deletion: A rare genetic disorder where a portion of chromosome 4 is deleted at a location called 16.3. The condition is characterized by malformations in most parts of the body as the deletion affects growth and development of the fetus. More detailed information about the symptoms, causes, and treatments of 4p16.3 deletion is available below.

Symptoms of 4p16.3 deletion

• Small head
• Congenital heart malformations
• Seizure
• Wide-set eyes
• Wide nasal bridge
• more symptoms...»

See full list of 38 symptoms of 4p16.3 deletion

Wrongly Diagnosed with 4p16.3 deletion?

• Failure to diagnose 4p16.3 deletion
• Undiagnosed: 4p16.3 deletion

4p16.3 deletion: Complications

Review possible medical complications related to 4p16.3 deletion:

• Early death (type of Death)
• Respiratory tract infections
• more complications...»

Less Common Symptoms of 4p16.3 deletion

• Protruding eyeballs
• Drooping eyelids
• Rieger anomaly
• Nystagmus
• Fused teeth
• more symptoms...»

See full list of 23 occasional symptoms of 4p16.3 deletion

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