4 results
diagnosis pediatrics symptoms 21hydroxylasedeficiency 21ohd alkaptonuria complications genetics
Psoriatic Arthritis: Pathogenesis and Clinical findings In tendons and connective tissues: • Enthesitis - Pain/tenderness over
Psoriatic Arthritis ... Pathogenesis and Clinical ... IP joints #PsoriaticArthritis ... #pathophysiology ... #diagnosis #signs
Psoriatic Arthritis: Complications • Ocular - Inflammation of middle layer of the eye (the uvea, which
Psoriatic Arthritis ... insufficiency #PsoriaticArthritis ... #pathophysiology ... #diagnosis #signs
Alkaptonuria (Black Urine Disease) Urine turns dark when left standing due to oxidation of homogentisic acid Clinical
homogentisic acid Clinical ... • Ochronotic arthritis ... #Alkaptonuria #BlackUrine ... #Peds #Pediatrics ... #Diagnosis #Pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
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