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diagnosis neurology treatment pathophysiology differential urology comparison endocrinology palsy sclerosis 21hydroxylasedeficiency 21ohd acquired allergy als amyotrophic anaphylaxis arteritis benign bph
Bell's palsy There are many different causes of Facial Nerve Palsy. However, the commonest cause of unilateral facial
are many different ... causes of Facial ... the commonest cause ... #Palsy #Neurology ... #Signs #Symptoms
Gowers' Sign on Physical Exam Caused by proximal muscle weakness typically seen in muscular dystrophy #Gowers #Sign #PhysicalExam
Gowers' Sign on ... Physical Exam Caused ... #Gowers #Sign ... #PhysicalExam #neurology ... clinical #video #pediatrics
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 Multiple Sclerosis - Summary Multiple Sclerosis (MS) is an autoimmune-mediated neurodegenerative disease of the central nervous system
Examination: • UMN signs ... Clonus, Babinski’s sign ... • Lhermitte’s sign ... pupillary defect SIGNS ... Signs and symptoms
Bell's Palsy - Diagnosis and Management Summary - GrepMed Handbook Acute Idiopathic Unilateral Facial Nerve (CN7) Palsy Presentation:
Bell's Palsy - Diagnosis ... ophthalmoplegia), systemic signs ... Imaging (if atypical symptoms ... CNS inflammatory cause ... #Treatment #Neurology
Diabetic Ketoacidosis (DKA) - Pathogenesis and Clinical Findings • Note: in DKA, body K+ is lost
diffusion of K+ out of cells ... may cause serum ... renal function/urine ... Signs/Symptoms/Complications ... Abdominal pain, nausea
Generalized Seizures and Pseudoseizures Generalized seizures "are conceptualized as originating as some point within, and rapidly engaging,
lateralization are ... general seizure caused ... and metabolic causes ... Classification #Diagnosis #Neurology ... #Signs #Symptoms
Amyotrophic Lateral Sclerosis (ALS) Summary ALS: combination of the clinical examination finding of amyotrophy with the pathologic
of UMN and LMN signs ... of UMN and LMN signs ... both UMN and LMN signs ... EMG: LMN Signs in ... Lateral #Sclerosis #neurology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... males at birth due ... Signs/Symptoms/Complications ... non-arousable, decr urine ... endocrinology #peds #pediatrics
Trendelenburg Gait: Pathogenesis and clinical findings Skeletal Pathology of the Hip • Arthritis • Congenital hip dysplasia
Chondrodysplasia Neurologic ... position of knee due ... pathophysiology #causes ... #symptoms #signs
Benign Prostatic Hyperplasia: Pathogenesis and Clinical Findings Hormonal alterations (result of aging process) ->
diet, hormones, urine ... outlet obstruction due ... Chronic retention of urine ... Pathophysiology #Urology ... #Signs #Symptoms
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