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Pediatrics, neurology. Acute cerebellar ataxia of childhood is a childhood condition characterized by an unsteady gait, most likely secondary to an autoimmune response to infection, drug induced or paraneoplastic. [1] The most common viruses causing acute cerebellar ataxia are chickenpox virus and Epstein–Barr virus, leading to a childhood ...
Nystagmus. Nystagmus is a condition of involuntary (or voluntary, in some cases) [1] eye movement. [2] People can be born with it but more commonly acquire it in infancy or later in life. In many cases it may result in reduced or limited vision. [3] In normal eyesight, while the head rotates about an axis, distant visual images are sustained by ...
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 ...
Exterior of labyrinth of the inner ear. Benign paroxysmal positional vertigo ( BPPV) is a disorder arising from a problem in the inner ear. [ 3] Symptoms are repeated, brief periods of vertigo with movement, characterized by a spinning sensation upon changes in the position of the head. [ 1] This can occur with turning in bed or changing ...
ICD-9-CM. 95.44. MedlinePlus. 003429. In medicine, the caloric reflex test (sometimes termed 'vestibular caloric stimulation ') is a test of the vestibulo-ocular reflex that involves irrigating cold or warm water or air into the external auditory canal. This method was developed by Robert Bárány, who won a Nobel prize in 1914 for this discovery.
Dissociated vertical deviation. Dissociated vertical deviation ( DVD) is an eye condition which occurs in association with a squint, typically infantile esotropia. The exact cause is unknown, although it is logical to assume it is from faulty innervation of eye muscles.
Spinocerebellar ataxia type 1. Spinocerebellar ataxia type 1 (SCA1) is a rare autosomal dominant disorder, which, like other spinocerebellar ataxias, is characterized by neurological symptoms including dysarthria, hypermetric saccades, and ataxia of gait and stance. This cerebellar dysfunction is progressive and permanent.
One in three children up to 12 years old registered as missing in the U.S. over the last two decades is Hispanic, according to an analysis of official records by Noticias Telemundo.