11 results
diagnosis pediatrics disease endocrinology management symptoms 21hydroxylasedeficiency 21ohd agammaglobulinemia amyotrophic brudzinskis cellulitis chloride differential evaluation genetics glftap hypochloremia immunology incomplete
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Passive neck flexion causes ... While the pathophysiology ... flexion occurs as ... #Meningitis #Clinical ... PhysicalExam #Pediatrics #Peds
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 Hypochloremia - Differential Diagnosis Algorithm Cause - Decreased Intake: • Low salt in diet • Exclusive D5W
Differential Diagnosis Algorithm ... Cause - Decreased ... - Gitelman SIGNS ... Hypotension • AMS ... #Pathophysiology
Orbital Cellulitis: Pathogenesis and Clinical Findings Definitions: a. Chemosis: Edema of the bulbar conjunctiva b. Panopthalmitis: inflammation of all
Pathogenesis and Clinical ... pupillary defect -> Decreased ... thrombosis -> Meningitis ... Orbital #Cellulitis #pathophysiology ... ophthalmology #diagnosis #signs
Amyotrophic Lateral Sclerosis (ALS) Summary ALS: combination of the clinical examination finding of amyotrophy with the pathologic
of the clinical ... lateral sclerosis Pathophysiology ... cellular function Clinical ... - Causes progressive ... - Fatigue and decreased
Pituitary Mass Effects - Pathogenesis and Clinical Findings • Pituitary turnors are almost always a benign
Pathogenesis and Clinical ... of all sizes, it ... Signs / Symptoms ... Post-nasal drip • Meningitis ... mnemonic #GLFTAP #pathophysiology
X-Linked Agammaglobulinemia: Pathogenesis and clinical findings The epidemiology of this disease is 1/340,000 births and roughly double
Pathogenesis and clinical ... Signs of immunodeficiency ... Inability to produce all ... humoral immunity Signs ... Agammaglobulinemia #XLinked #pathophysiology
Pott's Disease in Tuberculosis - Diagnosis and Management Summary Epidemiology: - Typically from TB endemic areas -
extrapulmonary cases ... Clinical Signs ... pain, numbness, decreased ... reflexes Pathophysiology ... should be done in ALL
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... • This is also ... Signs/Symptoms/Complications ... endocrinology #peds
Mastoiditis: Pathogenesis and clinical findings Acute or Chronic Otitis Media -> Stage 1: Hyperemeia of the mastoid
Pathogenesis and clinical ... increases causing decreased ... cortical bone -> Meningitis ... #Mastoiditis #pathophysiology ... #signs #symptoms
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
if they have no clinical ... , elevation of ALT ... lack of tapering, decreased ... and lab signs ( ... #Diagnosis #Peds
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