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Total recorded alcohol consumption per capita of individuals 15 years or older, in liters of pure alcohol. Alcoholism is the main cause of alcoholic polyneuropathy. In 2020 the NIH quoted an estimate that in the United States 25% to 66% of chronic alcohol users experience some form of neuropathy. [ 7 ]
Dysdiadochokinesia is a feature of cerebellar ataxia and may be the result of lesions to either the cerebellar hemispheres or the frontal lobe (of the cerebrum), it can also be a combination of both. [3]
Adjustment disorder, with mixed anxiety and depressed mood: 309.4: Adjustment disorder, with mixed disturbance of emotions and conduct: V71.01: Adult antisocial behavior: 995.2: Adverse effects of medication NOS: 780.9: Age-related cognitive decline: 300.22: Agoraphobia without history of panic disorder: 305.00: Alcohol abuse: 303.90: Alcohol ...
291.0 Alcohol withdrawal delirium; 291.2 Alcohol-induced persisting dementia; 291.1 Alcohol-induced persisting amnestic disorder; 291.x Alcohol-induced psychotic disorder.5 With delusions.3 With hallucinations; 291.89 Alcohol-induced mood disorder (coded 291.8 in the DSM-IV) 291.89 Alcohol-induced anxiety disorder (coded 291.8 in the DSM-IV)
In North America and Australia, DSM-5 criteria are used for diagnosis, while European countries usually use the ICD-10. The DSM-IV criteria for diagnosis of ADHD is 3–4 times more likely to diagnose ADHD than is the ICD-10 criteria. [217] ADHD is alternately classified as neurodevelopmental disorder [218] or a disruptive behaviour disorder ...
The DSM-5 allows for diagnosis of the predominantly inattentive presentations of ADHD (ICD-10 code F90.0) if the individual presents six or more (five for adults) of the following symptoms of inattention for at least six months to a point that is disruptive and inappropriate for developmental level:
Attention-deficit hyperactivity disorder (with hyperactivity) 314.01 F90 Tic disorders (involuntary, compulsive, repetitive, stereotyped) F95 Tourette's syndrome: F95.2 Stereotypic movement disorder: F98.5 Huntington's disease (Huntington's chorea) 333.4 G10 Dystonia: G24 Drug induced dystonia: G24.0 Idiopathic familial dystonia 333.6 G24.1
Patients with hereditary motor and sensory neuropathies are diagnosed through a physical evaluation that looks for muscle atrophy, weakness, and sensory responses. [3] In addition to this, electromyography and motor nerve conduction tests can help clinicians decide what type of motor and sensory neuropathy it is and how severe the disease is.