NEUROLOGY

Pediatric Neurology

Sep 7, 2016 by in NEUROLOGY Comments Off on Pediatric Neurology

Pediatric Neurology QUESTIONS 1. A 5-year-old boy presents to the clinic with a history of epilepsy, cognitive regression, and progressive blindness. A skin biopsy is done and demonstrates intracellular accumulation…

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Behavioral Neurology and Dementia

Sep 7, 2016 by in NEUROLOGY Comments Off on Behavioral Neurology and Dementia

Behavioral Neurology and Dementia QUESTIONS 1. What percentage of people in the United States older than 80 have Alzheimer’s dementia (AD)? A. 5% B. 25% C. 40% D. 75% E….

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Stupor and Coma

Sep 7, 2016 by in NEUROLOGY Comments Off on Stupor and Coma

Stupor and Coma QUESTIONS 1. A 76-year-old male presents with the inability to maintain attention. He is easily distracted, fidgety, and occasionally mistakes the wires in the room for snakes….

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Sleep Medicine

Sep 7, 2016 by in NEUROLOGY Comments Off on Sleep Medicine

Sleep Medicine QUESTIONS 1. What percentage of Americans suffer from insomnia (both acute and chronic)? A. 10% B. 40% C. 90% D. <1% E. None of the above View Answer…

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Headache

Sep 7, 2016 by in NEUROLOGY Comments Off on Headache

Headache QUESTIONS 1. What are the classic symptoms associated with migraine headaches? A. Anxiety B. Numbness C. Throbbing D. None of the above View Answer 1. Answer: C. Throbbing. Although…

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Anatomy and Physiology

Sep 7, 2016 by in NEUROLOGY Comments Off on Anatomy and Physiology

Anatomy and Physiology QUESTIONS 1. The diencephalon consists of all of the following structures except: A. thalamus B. subthalamus C. pons D. putamen E. all of the above View Answer…

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Myoglobinuric Syndromes Including Malignant Hyperthermia

Sep 2, 2016 by in NEUROLOGY Comments Off on Myoglobinuric Syndromes Including Malignant Hyperthermia

Myoglobinuria—the presence in urine of a 17.8-kDa, red pigment, iron-protein compound called myoglobin—results from rhabdomyolysis, which is the acute breakdown or necrosis of skeletal muscle fibers whose contents (among them…

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Metabolic and Mitochondrial Myopathies

Sep 2, 2016 by in NEUROLOGY Comments Off on Metabolic and Mitochondrial Myopathies

McArdle disease, an autosomal recessive myophosphorylase deficiency leading to glycolytic defects, is the common glycogen storage disease (GSD). Other glycolytic defects—phosphofructokinase, phosphoglycerate mutase, and lactic dehydrogenase deficiencies—produce similar clinical pictures….

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Endocrine, Toxic, and Critical Illness Myopathies

Sep 2, 2016 by in NEUROLOGY Comments Off on Endocrine, Toxic, and Critical Illness Myopathies

Hypothyroid Myopathy. Most patients with myxedema (chronic hypothyroidism) complain of weakness; 25% have objective proximal muscle weakness. Myoedema, an electrically silent mounding of percussed muscle, occurs in one third of…

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Myopathies: Hypokalemia/Hyperkalemia and the Periodic Paralyses Channelopathies Myopathies Associated with Disorders of Potassium Metabolism

Sep 2, 2016 by in NEUROLOGY Comments Off on Myopathies: Hypokalemia/Hyperkalemia and the Periodic Paralyses Channelopathies Myopathies Associated with Disorders of Potassium Metabolism

Hypokalemia-associated weakness does not usually become problematic until potassium levels fall toward and then below 1.5 mEq/L, with mild weakness, fatigue, and muscle cramping giving way to severe and generalized…

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