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Hereditary Spastic Paraplegia 87
A hereditary spastic paraplegia characterized by infantile or early childhood onset of lower limb spasticity that is caused by homozygous or compound heterozygous mutation in the TMEM63C gene on chromosome 14q24.3.
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.
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Overview
A hereditary spastic paraplegia characterized by infantile or early childhood onset of lower limb spasticity that is caused by homozygous or compound heterozygous mutation in the TMEM63C gene on chromosome 14q24.3.
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.