5 results
diagnosis genetics pediatrics 21hydroxylasedeficiency 21ohd algorithm anteriorischemicopticneuropathy disease endocrinology gca giantcellarteritis management msk ophthalmology potts praderwilli rheumatology spondylolisthesis spondylolysis summary
Spondylolysis & Spondylolisthesis: Pathogenesis and Clinical Findings Pars interarticularis stress fracture (spondylolysis) - most frequently in the
Pathogenesis and Clinical ... XR — scotty dog sign ... vertebrae • CT ... MSK #diagnosis #pathophysiology ... #signs #symptoms
Anterior ischemic optic neuropathy (AION) - Recognition of giant cell arteritis (GCA) 1) Is visual loss caused
optic neuropathy (AION ... thrombosis of short ... Clinical manifestations ... Doppler US : halo sign ... PET/CT: aortitis
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... /Symptoms/Complications ... fractures • Short ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Pott's Disease in Tuberculosis - Diagnosis and Management Summary Epidemiology: - Typically from TB endemic areas -
extrapulmonary cases Clinical ... Signs/Symptoms: ... years - May have signs ... decreased reflexes Pathophysiology ... involvement - CT
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... maintains appropriate ion ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds
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