4 results
diagnosis 21hydroxylasedeficiency 21ohd anteriorischemicopticneuropathy cord differential disease endocrinology gca genetics giantcellarteritis incomplete kawasaki neurology ophthalmology pathophysiology rheumatology spinal spinalcord
Anterior ischemic optic neuropathy (AION) - Recognition of giant cell arteritis (GCA) 1) Is visual loss caused
Is visual loss caused ... acute ischemic disorder ... Clinical manifestations ... Doppler US : halo sign ... Ophthalmology #Diagnosis #Algorithm
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 ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
if they have no clinical ... lack of tapering, decreased ... and lab signs ( ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
Spinal Cord Disorders - Differential Diagnosis Framework Spinal cord neurological lesion: Clinical findings: • Symptoms and signs below
neurological lesion: Clinical ... • Symptoms and signs ... Cauda equina- decreased ... Non-compressive Spinal Cord Causes ... differential #algorithm
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