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Year : 2004  |  Volume : 52  |  Issue : 3  |  Page : 363--364

Beckerís variant of myotonia congenita in two siblings- A clinico-genetic study

Kalyan B Bhattacharyya, P Sengupta, S Basu, NP Bhattacharya 
 Department of Neurology, Calcutta National Medical College & Hospital, 24 Gorachand Road, Calcutta - 700 014, India

Correspondence Address:
Kalyan B Bhattacharyya
Department of Neurology, Calcutta National Medical College & Hospital, 2/V Cornfield Road, Kolkata - 700 019
India

We report a family of a brother and sister of myotonia congenita, conforming to autosomal recessive transmission (Beckerís variety). To the best of our knowledge, no account of a family of autosomal recessive myotonia (Beckerís disease), has earlier been reported from India.


How to cite this article:
Bhattacharyya KB, Sengupta P, Basu S, Bhattacharya N P. Beckerís variant of myotonia congenita in two siblings- A clinico-genetic study.Neurol India 2004;52:363-364


How to cite this URL:
Bhattacharyya KB, Sengupta P, Basu S, Bhattacharya N P. Beckerís variant of myotonia congenita in two siblings- A clinico-genetic study. Neurol India [serial online] 2004 [cited 2020 Jul 7 ];52:363-364
Available from: http://www.neurologyindia.com/article.asp?issn=0028-3886;year=2004;volume=52;issue=3;spage=363;epage=364;aulast=Bhattacharyya;type=0