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  2. Rigid spine syndrome - Wikipedia

    en.wikipedia.org/wiki/Rigid_spine_syndrome

    Rigid spine syndrome, also known as congenital muscular dystrophy with rigidity of the spine (CMARS), is a rare and often debilitating neuromuscular disorder.It is characterized by progressive muscle stiffness and rigidity, particularly in the spine, which can severely limit mobility and impact quality of life.

  3. Hypotonia - Wikipedia

    en.wikipedia.org/wiki/Hypotonia

    Hypotonia is a state of low muscle tone [1] (the amount of tension or resistance to stretch in a muscle), often involving reduced muscle strength. Hypotonia is not a specific medical disorder, but a potential manifestation of many different diseases and disorders that affect motor nerve control by the brain or muscle strength.

  4. Spastic cerebral palsy - Wikipedia

    en.wikipedia.org/wiki/Spastic_cerebral_palsy

    People with the spastic type of CP typically have muscles that are "tight" or stiff due to high muscle tone. [2] Symptoms of spastic cerebral palsy vary as the disability can affect individuals differently. [2] However, they typically appear in infancy and early childhood and most children are diagnosed in the first two years of life. [7]

  5. Congenital muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Congenital_muscular_dystrophy

    CMD with brain-eye, also called muscle-eye-brain disease, [19] is a rare form of congenital muscular dystrophy (autosomal recessive disorder) causing a lack of normal muscle tone which can delay walking due to being weak, also paralysis of eye muscles and intellectual disability which affects an individual's way of processing information. [19]

  6. Cerebral palsy - Wikipedia

    en.wikipedia.org/wiki/Cerebral_palsy

    Cerebral palsy (CP) is a group of movement disorders that appear in early childhood. [1] Signs and symptoms vary among people and over time, [1] [3] but include poor coordination, stiff muscles, weak muscles, and tremors. [1] There may be problems with sensation, vision, hearing, and speech. [1]

  7. Myotonia congenita - Wikipedia

    en.wikipedia.org/wiki/Myotonia_congenita

    Myotonia congenita is a congenital neuromuscular channelopathy that affects skeletal muscles (muscles used for movement). It is a genetic disorder.The hallmark of the disease is the failure of initiated contraction to terminate, often referred to as delayed relaxation of the muscles and rigidity. [1]

  8. Management of cerebral palsy - Wikipedia

    en.wikipedia.org/wiki/Management_of_cerebral_palsy

    Botulinum toxin is focal treatment, meaning that a limited number of muscles can be injected at the same time. The effect of the toxin is reversible and a reinjection may be needed every 4–6 months. [61] In children it decreases spasticity and improve range of motion and thus has become commonly used. [59] [60] [62] Botulin toxin has been ...

  9. Congenital myasthenic syndrome - Wikipedia

    en.wikipedia.org/wiki/Congenital_myasthenic_syndrome

    Postsynaptic symptoms in infants include severe muscle weakness, feeding and respiratory problems, and delays in the ability to sit, crawl, and walk. Synaptic symptoms include early childhood feeding and respiratory problems, reduced mobility, curvature of the spine, and weakness, which causes a delay in motor milestones.