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Hypomyelinating Leukodystrophy 16
A hypomyelinating leukodystrophy characterized by onset of hypotonia, nystagmus, and mildly delayed motor development in infancy that is caused by heterozygous mutation in the TMEM106B gene on chromosome 7p21.
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
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Overview
A hypomyelinating leukodystrophy characterized by onset of hypotonia, nystagmus, and mildly delayed motor development in infancy that is caused by heterozygous mutation in the TMEM106B gene on chromosome 7p21.
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.