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  2. Inclusion body myositis - Wikipedia

    en.wikipedia.org/wiki/Inclusion_body_myositis

    Common early symptoms include frequent tripping and falling and difficulty going up stairs. Foot drop in one or both feet can occur. [14] Part of the cause for this dysfunction is the early involvement of the quadriceps muscles. [1] Weakness of the tibialis anterior muscle is responsible for foot drop. Another common early symptom is trouble ...

  3. Myokymia - Wikipedia

    en.wikipedia.org/wiki/Myokymia

    Myokymia is an involuntary, spontaneous, localized quivering of a few muscles, or bundles within a muscle, but which are insufficient to move a joint. One type is superior oblique myokymia . Myokymia is commonly used to describe an involuntary eyelid muscle contraction, typically involving the lower eyelid or less often the upper eyelid .

  4. Superior oblique myokymia - Wikipedia

    en.wikipedia.org/wiki/Superior_oblique_myokymia

    Superior oblique myokymia is a neurological disorder affecting vision and was named by Hoyt and Keane in 1970. [1] It is a condition that presents as repeated, brief episodes of movement, shimmering or shaking of the vision of one eye, a feeling of the eye trembling, or vertical/tilted vision. It can present as one or more of these symptoms.

  5. Neuromyotonia - Wikipedia

    en.wikipedia.org/wiki/Neuromyotonia

    NMT is a diverse disorder. As a result of muscular hyperactivity, patients may present with muscle cramps, stiffness, myotonia-like symptoms (slow relaxation), associated walking difficulties, hyperhidrosis (excessive sweating), myokymia (quivering of a muscle), fasciculations (muscle twitching), fatigue, exercise intolerance, myoclonic jerks and other related symptoms.

  6. Myositis - Wikipedia

    en.wikipedia.org/wiki/Myositis

    For myositis caused by a medication, it is important to stop using that medication. [4] There are a variety of treatment options available if myositis is caused by an autoimmune disease. Glucocorticoids are often the first choice for treatment. [10] This drug works to weaken the immune system so that it is not able to attack the muscles.

  7. Autosomal recessive axonal neuropathy with neuromyotonia

    en.wikipedia.org/wiki/Autosomal_recessive_axonal...

    This condition was discovered in 1991 by Hahn et al., when they described two Chinese-Canadian siblings of the opposite sex. The male had difficulties releasing his grip, childhood-onset neuromyotonia and muscle stiffness, progressive motor neuropathy, finger cramping while and after writing, involuntary twitches of the finger, thigh and forearm muscles, foot drop-associated gait problems ...

  8. Morvan's syndrome - Wikipedia

    en.wikipedia.org/wiki/Morvan's_syndrome

    Morvan's syndrome is a rare, life-threatening autoimmune disease named after the nineteenth century French physician Augustin Marie Morvan. "La chorée fibrillaire" was first coined by Morvan in 1890 when describing patients with multiple, irregular contractions of the long muscles, cramping, weakness, pruritus, hyperhidrosis, insomnia and delirium. [1]

  9. Episodic ataxia - Wikipedia

    en.wikipedia.org/wiki/Episodic_ataxia

    Episodic ataxia (EA) is an autosomal dominant disorder characterized by sporadic bouts of ataxia (severe discoordination) with or without myokymia (continuous muscle movement). There are seven types recognized but the majority are due to two recognized entities. [ 1 ]