Search results
Results From The WOW.Com Content Network
Ataxia–telangiectasia (AT or A–T), also referred to as ataxia–telangiectasia syndrome or Louis–Bar syndrome, [1] is a rare, neurodegenerative disease causing severe disability. Ataxia refers to poor coordination and telangiectasia to small dilated blood vessels, both of which are hallmarks of the disease. [ 2 ]
Codes following these are found at List of MeSH codes (C11). For other MeSH codes, ... MeSH C10.228.140.252.190.530.060 – ataxia telangiectasia;
Acquired telangiectasia, not related to other venous abnormalities, for example on the face and trunk, can be caused by factors such as Cushing's syndrome; Rosacea; Blepharitis [9] Environmental damage such as that caused by sun [10] or cold exposure; Age [10] Trauma to skin such as contusions or surgical incisions.
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.
Patients with ataxia telangiectasia have prolonged vertical and horizontal saccade latencies and hypometric saccades, and, although not all, some patients show head thrusts. [ 3 ] [ 10 ] [ 12 ] Diagnosis
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 . The condition typically manifests in childhood or adolescence, with initial ...
Autosomal dominant cerebellar ataxia; Other names: Autosomal dominant spinocerebellar ataxia [1] Autosomal dominant is the manner in which this condition is inherited: Symptoms: Multi system involvement [2] Types: ADCS type1, ADCA type 2, ADCA type 3 [2] Diagnostic method: MRI, CT scan [3] Treatment: Anticonvulsants may be used [2]
The features of this condition include: [citation needed] Facial dysmorphism; Short stature; Mild motor control and learning difficulties; Mild ataxia; Microcephaly; Normal intelligence