\"NKX2-1 Syndrome\" \u2013\u00a0What Is It?<\/h2><\/div>
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NKX2-1 syndrome is a disease caused by pathogenic variants<\/span>, i.e., genetic changes in the NKX2-1<\/em> gene. It can manifest itself clinically in different forms: In the complete picture of brain-lung-thyroid syndrome, all three organs are affected, but a combination of manifestations in the brain and thyroid gland or an isolated movement disorder with involuntary, irregular and jerky movements, so-called benign hereditary chorea, can also occur.<\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div>
Overview of the Chapters on This Page:<\/h4><\/div><\/div><\/div>
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NKX2-1 Syndrome \u2013 What Is It? (This Section)<\/div><\/li><\/ul><\/div><\/div>