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Craniolenticulosutural Dysplasia
A syndrome in neonates that is characterized by facial dysmorphism, late-closing fontanels, cataract, and skeletal defects. It is caused by the mutation of the SEC23A gene on the 14th chromosome, with the underproduction
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 in neonates that is characterized by facial dysmorphism, late-closing fontanels, cataract, and skeletal defects. It is caused by the mutation of the SEC23A gene on the 14th chromosome, with the underproduction
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.