Benign (non-paroxysmal) familial chorea. Paediatric perspectives.
نویسندگان
چکیده
We describe a non-progressive choreo-athetoid disorder of early onset, present in three families. There were no appreciable abnormalities in pregnancy, during the perinatal period, or in infancy. In each case the family history suggested transmission as an autosomal dominant trait, the gene showing diminished penetrance. Other families have been reported with the disorder and such titles as benign familial chorea, familial essential (benign chorea, or hereditary non-progressive chorea of early onset have been given to it. Our experience suggests that this is not a rare disorder, and that it is one likely to present in the paediatric age group; correct diagnosis is important so that unnecessary investigations are not undertaken, genetic counselling can be given, and proper management advice offered to families and schools.
منابع مشابه
Benign familial infantile convulsions: a clinical study of seven Dutch families.
Benign familial infantile convulsions (BFIC) is a recently identified partial epilepsy syndrome with onset between 3 and 12 months of age. We describe the clinical characteristics and outcome of 43 patients with BFIC from six Dutch families and one Dutch-Canadian family and the encountered difficulties in classifying the syndrome. Four families had a pure BFIC phenotype; in two families BFIC wa...
متن کاملBenign familial chorea: an association with intellectual impairment.
Twenty-four members of a family with benign familial chorea underwent testing for evidence of intellectual impairment. Lower verbal intelligence was found in affected individuals compared to unaffected family members, as were deficits in verbal abstract concept formation. These results challenge the notion that benign familial chorea uniformly spares the intellect in all kindreds.
متن کاملChild Neurology: PRRT2-associated movement disorders and differential diagnoses.
Paroxysmal kinesigenic dyskinesia (PKD) (MIM 128200) is a rare paroxysmal movement disorder that occurs at an estimated prevalence of 1:150,000 individuals. Onset is most commonly in childhood or adolescence, with sporadic and familial cases being reported. PKD is characterized by short and frequent episodes of dystonic or choreiform movements that are precipitated by sudden voluntary movements...
متن کاملADCY5 Mutations and Benign Hereditary Chorea
Investigators from the Institute of Neurology, London, UK, and centers in Italy, Germany, and Greece, studied 18 unrelated cases of benign hereditary chorea BHC (7 familial, 11 sporadic) who were negative for NKX2-1 mutations.
متن کاملMicrodeletions detected using chromosome microarray in children with suspected genetic movement disorders: a single-centre study.
AIM Chromosome microarray (CMA) can determine copy number variants such as microdeletions or microduplications. Microdeletions of movement disorder genes including epsilon-sarcoglycan (SGCE) and thyroid transcription factor-1 (TITF1) have been described in patients with myoclonus dystonia and benign hereditary chorea respectively. We examined whether CMA is a valuable tool in the investigation ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Archives of disease in childhood
دوره 56 8 شماره
صفحات -
تاریخ انتشار 1981