6 results
peds diagnosis genetics 21hydroxylasedeficiency 21ohd aorta aorticdissection aorticflap cardiacus clinical feedbackloop gh growthhormone ophthalmology otitismedia pituitary praderwilli suprasternalnotch syndrome typeb
Feedback Loop: Growth Hormone (GH) Growth Hormone: • Liver -> GHR activates JAK-STAT pathway -> Incr IGF1
activates lipolysis Signs ... /Symptoms: • GH ... deficiency: - Short ... #FeedbackLoop #endocrinology ... #pathophysiology
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
Xeropthalmia: Pathogenesis and Ocular Manifestations Decr Visual pigment -> Keratinization, thickening & non-wetting of the conjunctiva
mucins with reduced tear ... conjunctiva) • Bitot's spots ... #Xeropthalmia #pathophysiology ... ophthalmology #diagnosis #signs ... #symptoms
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
Air from middle ear ... in the middle ear ... #OtitisMedia #pathophysiology ... #diagnosis #symptoms ... #signs #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
This is a suprasternal notch view demonstrating an aortic flap in a patient with a Stanford
This 40ish year ... The POCUS allowed ... linear or fine parts ... with suspicious signs ... /symptoms allows
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