Community
Waisman Syndrome
A syndrome characterized by delayed psychomotor development, impaired intellectual development, and early-onset Parkinson disease that is caused by hemizygous or homozygous mutation in the RAB39B gene on chromosome Xq28.
This information is for educational purposes only and is not medical advice. Always consult your healthcare provider about your specific condition and treatment.
When to seek help
Seek medical help right away if you have severe, sudden, or worsening symptoms, trouble breathing, chest pain, or any symptom that feels life-threatening. This community is for peer support and education only and is not a substitute for professional medical advice.
If you are experiencing a medical emergency, contact your local emergency services immediately.
Overview
A syndrome characterized by delayed psychomotor development, impaired intellectual development, and early-onset Parkinson disease that is caused by hemizygous or homozygous mutation in the RAB39B gene on chromosome Xq28.
Resources
Join the Waisman Syndrome community
Talk with people who understand, share what helps, and find support from others living with waisman syndrome. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.