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Pontocerebellar Hypoplasia Type 10
A pontocerebellar hypoplasia that is characterized by severe developmental delays, progressive microcephaly, spasticity and seizure, is caused by autosomal recessive inheritance of mutation in the CLP1 gene.
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 pontocerebellar hypoplasia that is characterized by severe developmental delays, progressive microcephaly, spasticity and seizure, is caused by autosomal recessive inheritance of mutation in the CLP1 gene.
Resources
Join the Pontocerebellar Hypoplasia Type 10 community
Talk with people who understand, share what helps, and find support from others living with pontocerebellar hypoplasia type 10. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.