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  2. 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 ...

  3. Trendelenburg gait - Wikipedia

    en.wikipedia.org/wiki/Trendelenburg_gait

    Trendelenburg gait, first described by Friedrich Trendelenburg in 1895, [1] is an abnormal human gait caused by an inability to maintain the pelvis level while standing on one leg. It is caused by weakness or ineffective action of the gluteus medius and gluteus minimus muscles.

  4. Gait abnormality - Wikipedia

    en.wikipedia.org/wiki/Gait_abnormality

    Likewise, difficulty in walking due to arthritis or joint pains (antalgic gait) sometimes resolves spontaneously once the pain is gone. [3] [4] Hemiplegic persons have circumduction gait, where the affected limb moves through an arc away from the body, and those with cerebral palsy often have scissoring gait. [citation needed]

  5. Ataxia - Wikipedia

    en.wikipedia.org/wiki/Ataxia

    Ataxia (from Greek α- [a negative prefix] + -τάξις [order] = "lack of order") is a neurological sign consisting of lack of voluntary coordination of muscle movements that can include gait abnormality, speech changes, and abnormalities in eye movements, that indicates dysfunction of parts of the nervous system that coordinate movement, such as the cerebellum.

  6. Myopathic gait - Wikipedia

    en.wikipedia.org/wiki/Myopathic_gait

    The "waddling" is due to the weakness of the proximal muscles of the pelvic girdle. [1] The patient uses circumduction to compensate for gluteal weakness. [2] Conditions associated with a myopathic gait include pregnancy, congenital hip dysplasia, muscular dystrophies and spinal muscular atrophy.

  7. Flaccid paralysis - Wikipedia

    en.wikipedia.org/wiki/Flaccid_paralysis

    Flaccid paralysis is a neurological condition characterized by weakness or paralysis and reduced muscle tone without other obvious cause (e.g., trauma). [1] This abnormal condition may be caused by disease or by trauma affecting the nerves associated with the involved muscles.

  8. Myotonia - Wikipedia

    en.wikipedia.org/wiki/Myotonia

    Myotonia is a symptom of a small handful of certain neuromuscular disorders characterized by delayed relaxation (prolonged contraction) of the skeletal muscles after voluntary contraction or electrical stimulation, and the muscle shows an abnormal EMG. [1] [2]

  9. Friedreich's ataxia - Wikipedia

    en.wikipedia.org/wiki/Friedreich's_ataxia

    Often due to cardiac complications Friedreich's ataxia (FRDA) is a rare, inherited, autosomal recessive neurodegenerative disorder that primarily affects the nervous system, causing progressive damage to the spinal cord, peripheral nerves, and cerebellum, leading to impaired muscle coordination ( ataxia ).