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diagnosis 21hydroxylasedeficiency 21ohd amyotrophic anorexianervosa endocrinology genetics hypophosphatemia hypoxia lateral management neurology pediatrics peds phosphate psychiatry pulmonary respiratory sclerosis signs
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... glands • Salt wasting ... Signs/Symptoms/Complications ... Late (shock): cold ... #21HydroxylaseDeficiency #21OHD #pathophysiology
Amyotrophic Lateral Sclerosis (ALS) Summary ALS: combination of the clinical examination finding of amyotrophy with the pathologic
lateral sclerosis Pathophysiology ... disrupt cellular function ... multiple spinal cord ... - Causes progressive ... - Further testing
Hypophosphatemia and Hypoxia - Pathophysiology ↓ Phosphate leads to ↓ red cell 2,3-DPG and a reduction
and Hypoxia - Pathophysiology ... impacts respiratory function ... is a cause of refractory ... phosphorus is seen in COPD ... patients with COPD
Anorexia Nervosa: Complications CARDIAC ABNORMALITIES - Functional: Low BP, Sinus bradycardia, prolonged QT interval - Structural: Reduced
ABNORMALITIES - Functional ... Enzymes - From fasting ... Hypothermia and Cold ... mortality rates of all ... #pathophysiology
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