Literature DB >> 2964512

Hereditary progressive chorea without dementia.

W Schady1, R J Meara.   

Abstract

A family with hereditary non-Huntington's chorea is presented. Transmission was autosomal dominant with variable penetrance. Chorea commenced in childhood and affected predominantly the head, face and upper limbs. Dysarthria appeared later, followed in two family members by elements of an axial dystonia. There was no intellectual impairment. Unlike previously described families, symptoms progressed steadily up to the eighth decade, causing considerable physical disability.

Entities:  

Mesh:

Year:  1988        PMID: 2964512      PMCID: PMC1031549          DOI: 10.1136/jnnp.51.2.295

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  7 in total

1.  Hereditary nonprogressive chorea of early onset.

Authors:  A F Haerer; R D Currier; J F Jackson
Journal:  N Engl J Med       Date:  1967-06-01       Impact factor: 91.245

2.  Benign familial chorea with onset in childhood.

Authors:  R W Chun; R F Daly; B J Mansheim; G J Wolcott
Journal:  JAMA       Date:  1973-09-24       Impact factor: 56.272

3.  Benign, recessively inherited choreo-athetosis of early onset.

Authors:  P A Nutting; B R Cole; R N Schimke
Journal:  J Med Genet       Date:  1969-12       Impact factor: 6.318

4.  Benign (non-paroxysmal) familial chorea. Paediatric perspectives.

Authors:  G Sleigh; R H Lindenbaum
Journal:  Arch Dis Child       Date:  1981-08       Impact factor: 3.791

5.  Benign familial chorea: an association with intellectual impairment.

Authors:  D A Leli; T W Furlow; J C Falgout
Journal:  J Neurol Neurosurg Psychiatry       Date:  1984-05       Impact factor: 10.154

6.  Hereditary chorea without dementia.

Authors:  P O Behan; I Bone
Journal:  J Neurol Neurosurg Psychiatry       Date:  1977-07       Impact factor: 10.154

7.  Persistent rheumatic chorea.

Authors:  W R Gibb; A J Lees; J W Scadding
Journal:  Neurology       Date:  1985-01       Impact factor: 9.910

  7 in total
  6 in total

1.  Benign hereditary chorea of early onset maps to chromosome 14q.

Authors:  B B de Vries; W F Arts; G J Breedveld; J J Hoogeboom; M F Niermeijer; P Heutink
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

Review 2.  Benign Hereditary Chorea: An Update.

Authors:  Kathryn J Peall; Manju A Kurian
Journal:  Tremor Other Hyperkinet Mov (N Y)       Date:  2015-07-14

3.  Examination of Huntington's disease with atypical clinical features in a Bangladeshi family tree.

Authors:  Md Mahfuz Al-Mamun; Suprovath Kumar Sarker; Syeda Kashfi Qadri; Tahmina Shirin; Quazi Deen Mohammad; Regina LaRocque; Elinor K Karlsson; Narayan Saha; Muhammad Asaduzzaman; Firdausi Qadri; Md Kaiissar Mannoor
Journal:  Clin Case Rep       Date:  2016-11-11

4.  Altered pituitary morphology as a sign of benign hereditary chorea caused by TITF1/NKX2.1 mutations.

Authors:  Steffi Thust; Liana Veneziano; Michael H Parkinson; Kailash P Bhatia; Elide Mantuano; Cristina Gonzalez-Robles; Indran Davagnanam; Paola Giunti
Journal:  Neurogenetics       Date:  2022-01-25       Impact factor: 2.660

Review 5.  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.

Authors:  Liana Veneziano; Michael H Parkinson; Elide Mantuano; Marina Frontali; Kailash P Bhatia; Paola Giunti
Journal:  Cerebellum       Date:  2014-10       Impact factor: 3.847

Review 6.  Genetic disorders of thyroid metabolism and brain development.

Authors:  Manju A Kurian; Heinz Jungbluth
Journal:  Dev Med Child Neurol       Date:  2014-03-26       Impact factor: 5.449

  6 in total

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