3 results
diagnosis 21hydroxylasedeficiency alkaline alp biliary cholangitis cirrhosis genetics hyophosphatasia low pbc pediatrics phosphatase workup
Primary Biliary Cirrhosis (PBC) - Summary PBC Epidemiology: • Female:Male 9:1 • Common European descent • Age:
• Female:Male 9: ... 65 years PBC Pathophysiology ... PBC Signs and Symptoms ... or higher • Liver ... diagnosis #workup #hepatology
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
Low Alkaline Phosphatase - Hypophosphatasia Is Low Alkaline Phosphatase Of Clinical Importance? ALP enzyme- Discovered in 1923 Low
synthesized in: liver ... collection with EDTA Pathophysiology ... mineralization Symptoms ... • Elevation of urinary ... Hyophosphatasia #hepatology
No results found for "9 pathophysiology peds pathophysiology hepatology symptoms liver endocrinology primary 21ohd"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #9 #pathophysiology #peds #pathophysiology #hepatology #symptoms #liver #endocrinology #primary #21ohd