Community
Spondyloepimetaphyseal Dysplasia, Strudwick Type
A spondyloepimetaphyseal dysplasia that is caused by mutations in the COL2A1 gene which causes short stature and multiple skeletal abnormalities (lordosis, scoliosis, flattened vertebrae, pectus carinatum, coxa vara, clu
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 spondyloepimetaphyseal dysplasia that is caused by mutations in the COL2A1 gene which causes short stature and multiple skeletal abnormalities (lordosis, scoliosis, flattened vertebrae, pectus carinatum, coxa vara, clu
Resources
Join the Spondyloepimetaphyseal Dysplasia, Strudwick Type community
Talk with people who understand, share what helps, and find support from others living with spondyloepimetaphyseal dysplasia, strudwick type. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.