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Benign hereditary chorea

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Review Articles from PubMed

Review articles summarize what is currently known about a disease. They discuss research previously published by others. The terms "Benign hereditary chorea" returned 1 free, full-text review articles. First 1 results:
Benign hereditary chorea: a case report and brief review of inherited choreas.
Last Updated: Sep 30, 2014

Chorea as a nonprogressive abnormality is often associated with Sydenham chorea in the pediatric population. Benign hereditary chorea is a condition where chorea presents before age 5 years and runs a very slowly progressive course.

A novel de novo mutation of the TITF1/NKX2-1 gene causing ataxia, benign hereditary chorea, hypothyroidism and a pituitary mass in a UK family and review of the literature.
Last Updated: Nov 13, 2018

Benign hereditary chorea (BHC) is a rare autosomal dominant condition characterized by early onset, non-progressive chorea, usually caused by mutations in the thyroid transcription factor-1 gene (TITF1). We describe a novel mutation arising de novo in a proband presenting in infancy ...

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1 Free Review Articles 8 Review Articles

Editorials from PubMed

Editorial articles describe the outcome of a single study. They are the published results of original research. The terms "Benign hereditary chorea" returned 0 free, full-text editorial articles. First 0 results:
No publications were found for this category.
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Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "Benign hereditary chorea" returned 8 free, full-text research articles. First few results:
Benign hereditary chorea and deletions outside NKX2-1: What's the role of MBIP?
Last Updated: Dec 11, 2018

Heterozygous point mutations or deletions of the NKX2-1 gene cause benign hereditary chorea (BHC) or a various combinations of primary hypothyroidism, respiratory distress and neurological disorders. Deletions proximal to, but not encompassing, NKX2-1 have been described in few subjects ...

l-Thyroxine-responsive drop attacks in childhood benign hereditary chorea: A case report.
Last Updated: Aug 20, 2018

Benign hereditary chorea (BHC) is a rare autosomal dominant disease that is characterized by non-progressive chorea with early-childhood-onset, congenital hypothyroidism, and neonatal respiratory distress. Although tetrabenazine and levodopa are partly effective for chorea and drop ...

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8 Free Research Articles 45 Research Articles