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Myotonia congenita in a brother and sister
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2006; 16 (9): 604-605
in English | IMEMR | ID: emr-77519
ABSTRACT
Myotonia congenita is a rare channelopathy and carries a good prognosis. Two cases of young siblings are presented detected with difficulty in gait and motor activities. Both had typical hypertrophied body musculature. EMG was diagnostic
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Index: IMEMR (Eastern Mediterranean) Main subject: Siblings / Electromyography / Hypertrophy / Muscular Diseases Type of study: Case report Limits: Female / Humans / Male Language: English Journal: J. Coll. Physicians Surg. Pak. Year: 2006

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Index: IMEMR (Eastern Mediterranean) Main subject: Siblings / Electromyography / Hypertrophy / Muscular Diseases Type of study: Case report Limits: Female / Humans / Male Language: English Journal: J. Coll. Physicians Surg. Pak. Year: 2006