Teaching video neuroimages: cold-induced eyelid myotonia.
نویسندگان
چکیده
A 48-year-old man presented with episodic paraplegia and stiffness of hands, face, and tongue, along with eyelid myotonia when exposed to cold temperature, which he had since childhood. Eyelid myotonia was evoked either by exposure to cold weather (video on the Neurology® Web site at www.neurology.org and figure 1) or by forceful eye closure. Myotonia was elicited with percussion of the tongue and thenar eminence. EMG showed myotonic discharge at room temperature (figure 2). Creatine kinase was mildly elevated to 293 U/L. The genetic study showed missense mutation (R1448C) in the voltage-gated sodium channel, type IV, alpha subunit (SCN4A). The patient’s daughter had the same genetic mutation and similar symptoms. AUTHOR CONTRIBUTIONS The first author, Dr. Yi-Jen Wu, has done the work for the manuscript writing, clinical history taking, neurology exanimation, and the collections of all the laboratory examinations with the supervision of Dr. Chou-Ching Lin, the corresponding author.
منابع مشابه
Teaching video neuroimages: lid lag sign and diplopia in paramyotonia congenita.
Clinical bedside tests to provoke myotonia, such as eyelid closure, handgrip, and percussion myotonia, help to diagnose and differentiate myotonic disorders and prevent delayed genetic confirmation. Sodium channelopathies present with predominantly myotonia of the ocular muscles. In these cases, testing for myotonia of the upper eyelid and extraocular muscles could be of decisive diagnostic val...
متن کاملTeaching Video NeuroImages: sodium channel myotonia can present with stridor.
An 11-month-old girl presented with episodic severe stridor from birth, often resulting in cyanosis. Her parents had noted recurrent unilateral ptosis. Later she developed spasms of her hands during exercise. Psychomotor development was normal. Neurologic examination showed generalized hypertonia. Cerebral MRI excluded a Chiari malformation. Laryngoscopy under general anesthesia showed no abnor...
متن کاملTeaching video neuroimages: trapezius myotonia percussion sign in myotonic dystrophy type 2.
Myotonic dystrophy type 2 (DM2) is an autosomal dominant disorder with proximal weakness, muscle pain, and early-onset cataracts. In comparison with myotonic dystrophy type 1 (DM1), myotonia is less symptomatic, more proximal, and harder to detect during clinical and electrodiagnostic testing. Here we document the presence of trapezius myotonia in patients with DM2 (video on the Neurology® Web ...
متن کاملTeaching neuroimages: IgG4-related orbital disease and enlargement of the trigeminal nerve branches.
A 54-year-old man had a 5-year history of painless bilateral eyelid swelling, proptosis, and diplopia. MRI showed enlargement of extraocular muscles, lacrimal gland, and divisions of the trigeminal nerve (figure 1). Biopsy from the left infraorbital canal demonstrated lymphoplasmacytic infiltrate and fibrosis. Mean number of immunoglobulin G (IgG)41 cells was 155 per high-power field and ratio ...
متن کاملTeaching Video NeuroImages: epilepsy with myoclonic absences: a distinct electroclinical syndrome.
A 10-year-old girl presented with recurrent absence spells of 6 years’ duration. Video-EEG revealed absences with rhythmic unilateral shoulder jerks, classic of epilepsy with myoclonic absences (EMA) (videos 1 and 2 on the Neurology Web site at www.neurology.org; figure). The average age at onset is 7 years.1 EMA may be associated with trisomy 12p and Angelman syndrome.2 It has a variable progn...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Neurology
دوره 80 8 شماره
صفحات -
تاریخ انتشار 2013