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Ectodermal Dysplasia 13
An ectodermal dysplasia characterized by severe oligodontia accompanied by anomalies of hair and skin that is caused by homozygous or compound heterozygous mutation in the KREMEN1 gene on chromosome 22q12.1.
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
An ectodermal dysplasia characterized by severe oligodontia accompanied by anomalies of hair and skin that is caused by homozygous or compound heterozygous mutation in the KREMEN1 gene on chromosome 22q12.1.
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.