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21ohd acutelimbischemia ali cli embolectomy endocrinology endovascular genetics heparin hybridtherapy pediatrics peds thrombolysis thrombosis treatment
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Autosomal recessive mutation ... in CYP21A2 coding ... Signs/Symptoms/Complications ... a scrotum #21HydroxylaseDeficiency ... #21OHD #pathophysiology
Acute limb ischemia (ALI) Rapid decrease in lower limb blood flow due to acute occlusion of peripheral
are abrupt with pain ... pathophysiology: ... diseased arteries during ... angioplasty balloons, & stents ... #CLI #heparin #amputation
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