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A CASE OF SLOW CHANNEL CONGENTAL MYASTHENIC SYNDROME MOSES P MOORTHY

Journal: University Journal of Medicine and Medical Specialities (Vol.5, No. 2)

Publication Date:

Authors : ;

Page : 37-38

Keywords : Congenital Myasthenic Syndrome; Slow Channel; NMJ Disorder;

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Abstract

Congenital myasthenic syndrome are heterogenous inherited disorder characterized by impaired neuromuscular transmission. All are inherited as autosomal recessive manner except slow channel congenital myasthenic syndrome, which is inherited as autosomal dominant manner. It may manifest upto 5th to 6th decade. Here we are reporting a rare case of slow channel congenital myasthenic syndrome.

Last modified: 2019-03-29 15:50:52