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diagnosis signs management physicalexam differential disease genetics kawasaki meningitis pathophysiology timeline 21hydroxylasedeficiency 21ohd als amyotrophic bells brain cirrhosis clinical cns
Principal features of Destructive and Irritative cortical lesions in right-handed individual #Cortical #Cortex #Lesions #Features #Signs #Symptoms
Principal features ... of Destructive and ... Cortex #Lesions #Features ... #Signs #Symptoms ... #Brain #Neurology
Clinical Features and Complications of Measles Rash: Spreads downwards, from behind the ears to the whole Of the
Clinical Features ... and Complications ... Kopliks KoplikSpots #Peds ... #Pediatrics #Timeline ... #Signs #Symptoms
Kernig's Sign in Meningitis Kernig's sign is present if the patient, in the supine position with the
Kernig's Sign in ... Meningitis Kernig's sign ... position with the hip and ... #PhysicalExam #Pediatrics ... #Peds #neurology
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 Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features ... #PhysicalExam #Signs ... #Symptoms #Shock ... #Dehydration #Peds ... #Pediatrics
Kawasaki Disease (Mucocutaneous Lymph Node Syndrome) An rare systemic acute febrile vasculitic syndrome. Aetiology unknown. Affects
between 6 months and ... Kawasaki #Disease #Features ... #Signs #Symptoms ... #Diagnosis #Peds ... #Pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... /Symptoms/Complications ... Incr Skeletal fractures ... pathophysiology #peds ... #pediatrics
Kawasaki Disease - Timeline of Clinical Features and Complications - Fever >5 days - 4
Timeline of Clinical Features ... and Complications ... of the 5 other features ... #Signs #Symptoms ... #Peds #Pediatrics
Clinical features of Liver Disease in Children #Cirrhosis #LiverFailure #Signs #Symptoms #PhysicalExam #Findings #Diagnosis #Peds #Pediatrics #Hepatology **
Clinical features ... #LiverFailure #Signs ... #Symptoms #PhysicalExam ... Findings #Diagnosis #Peds ... #Pediatrics #Hepatology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
: Pathogenesis and ... Autosomal recessive mutation ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Bell's Palsy - Diagnosis and Management Summary - GrepMed Handbook Acute Idiopathic Unilateral Facial Nerve (CN7) Palsy Presentation:
4m • Atypical Features ... ophthalmoplegia), systemic signs ... presentation • Lyme Serology ... Imaging (if atypical symptoms ... Management #Treatment #Neurology
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