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: 2019-03-28
Authors : MOSES P MOORTHY;
Page : 37-38
Keywords : Congenital Myasthenic Syndrome; Slow Channel; NMJ Disorder;
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.
Other Latest Articles
- Carcinoma breast with rare sites of metastasis
- GRAPHIC ORGANIZER: A LEARNING TOOL IN TEACHING PHYSICAL SCIENCE
- ATYPICAL ,FULMINANT PRESENTATION OF SUBACUTE SCLEROSING PANENCEPHALITIS
- THEORETIC NUMBER BASIC METHODS OF INFORMATION TECHNOLOGIES FOR DIAGNOSTATION OF TECHNOLOGICAL OBJECTS OF THE OIL & GAS INDUSTRY
- YOUNG STROKE - MANIFESTATION OF DISULFIRAM-ETHANOL REACTION. A RARE CASE REPORT
Last modified: 2019-03-29 15:50:52