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A PRESENTATION  ON ABNORMAL MOVEMENT DISORDERS                                     Dr. Aarthy Joseph               Prof. Dr. Mageshkumar’s Unit
PATIENT1               PATIENT2 15 year, female, no family history             •60 year, female, known diabetic         1 week H/O abnormal movements•2 day H/O abnormal movements Systemic examination                                   •Systemic examination  Biochemical and hematological                  • RBS- 320, urine ketones- neg, Routine investigations- normal                            other investigations- normal • CXR and ECG- WNL                                           •CT brain • ASO titre- 200                                                    •Neurology opinion                                    •CT brain and MRI brain •Neurology opinion                                              •Cardiology opinion •Ophthalmology opinion •Serum ceruloplasmin •Urinary copper
DIAGNOSIS AND MANAGEMENT        PATIENT1                                 PATIENT2 RHEUMATIC CHOREA            HYPERGLYCEMIA INDUCED CHOREA TREATMENT Penicillin                                 Glycemic control with insulin Haloperidol                            Fluid correction
CHOREA ,[object Object]
Involuntary, rapid, irregular, jerky, purposeless, random, nonrhythmichyperkinesia
Present at rest, increased by activity, tension, emotional stress and self consciousness, and disappear in sleep
Most characteristic in the distal parts of upper extrimities,[object Object]
CAUSES Hereditary – Huntington’s disease, benign hereditary chorea, neuroacanthocytosis, dentatorubro-pallidoluysian atrophy Metabolic and endocrine disorders - Wilson disease, nonketotichyperglycemia, hypoglycemiahypobetalipoproteinemia, lipid storage diseases, Kernicterus, hyperthyroidism Paroxysmal - Paroxysmal kinesogenicchoreoathetosis, paroxysmal dystonicchoreoathetosis
[object Object],Drug induced - Neuroleptics, levodopa, oral contraceptives, cocaine, phenytoin Toxins - Alcohol intoxication and withdrawal, carbon monoxide, manganese, mercury Other choreas associated with systemic disease- SLE, antiphospholipid antibodies, Polycythemiavera,  AIDS Rarely- Stroke, Vascular malformation, tumours
RHEUMATIC CHOREA After infection with group A ß-hemolytic streptococcus 25% of cases of acute rheumatic fever  Average age of onset is 5-15 years Girls > boys According to the 1992 modification of the Jones criteria, chorea alone is sufficient for diagnosis of RF Imbalance among the dopaminergic system, intrastriatal cholinergic system, and inhibitory gamma-aminobutyric acid (GABA) system
Cross-reactivity between group A ß-hemolytic streptococcus and the basal ganglia Diagnosis of SC may be difficult. Chorea alone is sufficient for diagnosis providing other causes of the condition have been excluded ASO titre may be elevated Echocardiogram may show carditis Volumetric MRI shows enlargement of the basal ganglia in affected patients without other abnormalities Resolves spontaneously in 3-6 months Recurrences Treatment- Chronic Penicillin prophylaxis for 10 years Steroids Haloperidol, Valproate
CHOREA WITH NONKETOTIC HYPERGLYCEMIA  Focal neurological symptoms may provide the first clinical clue for the presence of non ketotichyperglycemia  Seizures, chorea, Chorea – ballismus syndrome  &focal neurological deficits Pathogenesis- depletion of GABA, Cerebral hypoperfusion T1 weighted MRI- hyperintense basal ganglia lesion SPECT studies- Striatalhypoperfusion and striatalhypometaboli Neurological symptoms improve with correction of hyperglycemia.

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Movement Disorders

  • 1. A PRESENTATION ON ABNORMAL MOVEMENT DISORDERS Dr. Aarthy Joseph Prof. Dr. Mageshkumar’s Unit
  • 2.
  • 3.
  • 4.
  • 5. PATIENT1 PATIENT2 15 year, female, no family history •60 year, female, known diabetic 1 week H/O abnormal movements•2 day H/O abnormal movements Systemic examination •Systemic examination Biochemical and hematological • RBS- 320, urine ketones- neg, Routine investigations- normal other investigations- normal • CXR and ECG- WNL •CT brain • ASO titre- 200 •Neurology opinion •CT brain and MRI brain •Neurology opinion •Cardiology opinion •Ophthalmology opinion •Serum ceruloplasmin •Urinary copper
  • 6. DIAGNOSIS AND MANAGEMENT PATIENT1 PATIENT2 RHEUMATIC CHOREA HYPERGLYCEMIA INDUCED CHOREA TREATMENT Penicillin Glycemic control with insulin Haloperidol Fluid correction
  • 7.
  • 8. Involuntary, rapid, irregular, jerky, purposeless, random, nonrhythmichyperkinesia
  • 9. Present at rest, increased by activity, tension, emotional stress and self consciousness, and disappear in sleep
  • 10.
  • 11. CAUSES Hereditary – Huntington’s disease, benign hereditary chorea, neuroacanthocytosis, dentatorubro-pallidoluysian atrophy Metabolic and endocrine disorders - Wilson disease, nonketotichyperglycemia, hypoglycemiahypobetalipoproteinemia, lipid storage diseases, Kernicterus, hyperthyroidism Paroxysmal - Paroxysmal kinesogenicchoreoathetosis, paroxysmal dystonicchoreoathetosis
  • 12.
  • 13. RHEUMATIC CHOREA After infection with group A ß-hemolytic streptococcus 25% of cases of acute rheumatic fever Average age of onset is 5-15 years Girls > boys According to the 1992 modification of the Jones criteria, chorea alone is sufficient for diagnosis of RF Imbalance among the dopaminergic system, intrastriatal cholinergic system, and inhibitory gamma-aminobutyric acid (GABA) system
  • 14. Cross-reactivity between group A ß-hemolytic streptococcus and the basal ganglia Diagnosis of SC may be difficult. Chorea alone is sufficient for diagnosis providing other causes of the condition have been excluded ASO titre may be elevated Echocardiogram may show carditis Volumetric MRI shows enlargement of the basal ganglia in affected patients without other abnormalities Resolves spontaneously in 3-6 months Recurrences Treatment- Chronic Penicillin prophylaxis for 10 years Steroids Haloperidol, Valproate
  • 15. CHOREA WITH NONKETOTIC HYPERGLYCEMIA Focal neurological symptoms may provide the first clinical clue for the presence of non ketotichyperglycemia Seizures, chorea, Chorea – ballismus syndrome &focal neurological deficits Pathogenesis- depletion of GABA, Cerebral hypoperfusion T1 weighted MRI- hyperintense basal ganglia lesion SPECT studies- Striatalhypoperfusion and striatalhypometaboli Neurological symptoms improve with correction of hyperglycemia.
  • 16. REFERENCES -DeJong’s The Nurological Examination -Harrison’s Principles of Internal Medicine -Web references from medscape