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  2. Acute cerebellar ataxia of childhood - Wikipedia

    en.wikipedia.org/wiki/Acute_cerebellar_ataxia_of...

    Signs and symptoms. Acute cerebellar ataxia usually follows 2–3 weeks after an infection. Onset is abrupt. Vomiting may be present at the onset but fever and nuchal rigidity characteristically are absent. Horizontal nystagmus is present in approximately 50% of cases. Truncal ataxia with deterioration of gait; Slurred speech and nystagmus ...

  3. Alström syndrome - Wikipedia

    en.wikipedia.org/wiki/Alström_syndrome

    Nystagmus (usually affects the children), one of the first symptoms to occur which causes involuntary rapid eye movement. Mild to moderate bilateral sensorineural hearing loss. Type 2 diabetes usually occurs in early childhood. Hyperinsulinemia/insulin resistance—development of high level of insulin in blood. Hypertriglyceridemia

  4. Nystagmus - Wikipedia

    en.wikipedia.org/wiki/Nystagmus

    Nystagmus as seen in a case of ocular albinism. The cause of pathological nystagmus may be congenital, idiopathic, or secondary to a pre-existing neurological disorder.It also may be induced temporarily by disorientation (such as on roller coaster rides or when a person has been spinning in circles) or by some drugs (alcohol, lidocaine, and other central nervous system depressants, inhalant ...

  5. Spinocerebellar ataxia - Wikipedia

    en.wikipedia.org/wiki/Spinocerebellar_ataxia

    Spinocerebellar ataxia ( SCA) is a progressive, degenerative, [ 1] genetic disease with multiple types, each of which could be considered a neurological condition in its own right. An estimated 150,000 people in the United States have a diagnosis of spinocerebellar ataxia at any given time. SCA is hereditary, progressive, degenerative, and ...

  6. 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] Ataxia can be provoked by psychological stress or startle, or heavy exertion ...

  7. Wolfram syndrome - Wikipedia

    en.wikipedia.org/wiki/Wolfram_syndrome

    Wolfram syndrome, also called DIDMOAD ( d iabetes i nsipidus, d iabetes m ellitus, o ptic a trophy, and d eafness), is a rare autosomal-recessive genetic disorder that causes childhood-onset diabetes mellitus, optic atrophy, and deafness as well as various other possible disorders including neurodegeneration.

  8. One and a half syndrome - Wikipedia

    en.wikipedia.org/wiki/One_and_a_half_syndrome

    Neuromyelitis optica spectrum disorder. Myasthenia Gravis. The one and a half syndrome is a rare weakness in eye movement affecting both eyes, in which one cannot move laterally at all, and the other can move only in outward direction. More formally, it is characterized by " a conjugate horizontal gaze palsy in one direction and an internuclear ...

  9. Vestibulocerebellar syndrome - Wikipedia

    en.wikipedia.org/wiki/Vestibulocerebellar_syndrome

    Vestibulocerebellar syndrome. Vestibulocerebellar syndrome, also known as vestibulocerebellar ataxia, is a progressive neurological disorder that causes a variety of medical problems. Initially symptoms present as periodic attacks of abnormal eye movements but may intensify to longer-lasting motor incapacity. The disorder has been localized to ...

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