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Congenital Nongoitrous Hypothyroidism 4
A congenital hypothyroidism characterized by a permanent thyroid deficiency present at birth and resulting from deficiency in TSH synthesis that is caused by homozygous mutation in the TSHB gene on chromosome 1p13.
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 congenital hypothyroidism characterized by a permanent thyroid deficiency present at birth and resulting from deficiency in TSH synthesis that is caused by homozygous mutation in the TSHB gene on chromosome 1p13.
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Join the Congenital Nongoitrous Hypothyroidism 4 community
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.