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diagnosis management liver oncology pediatrics syndrome 21hydroxylasedeficiency 21ohd aflp algorithm alkaline alp apml bariatric bypass calling cholangitis chronic cirrhosis cll
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Syndrome Signs/Symptoms ... /Complications: ... PraderWilli #Syndrome #genetics ... #pathophysiology ... #peds #pediatrics
The Liver Consult Primer - Guide to calling a consult HPI: - Start with reason for consult
- Cirrhosis & complications ... liver biopsy Meds ... - Outpatient meds ... Calling #Referral #Hepatology ... #Gastroenterology
Acute Fatty Liver of Pregnancy (AFLP) Pathophysiology: • Defect in fetal free fatty acid metabolism products →
Pregnancy (AFLP) Pathophysiology ... postpartum): • Initial symptoms ... Monitor and Treat Complications ... Liver #Pregnancy #hepatology ... diagnosis #management #pathophysiology
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
TRALI vs TACO - Transfusion Reactions TRALI: • Epidemiology: 0.1% of transfused patientsl • Risk factors: Critical
blood donor • Pathophysiology ... Criteria met without other ... ARDS to explain symptoms ... transfusion • Pathophysiology ... Transfusion #Reactions #hematology
Complications after Bariatric Surgery Post Bariatric Intestinal Failure: • Severe protein malnutrition after bariatric surgery • More
Complications after ... and vasomotor symptoms ... TypicallySilent via Emory Gastroenterology ... and Hepatology ... gastric #bypass #gastroenterology
Algorithm regarding the diagnosis and treatment of Hereditary Hemochromatosis HH. Step 1: In the patient with
suspected HH based on symptoms ... including liver and hematologic ... If other causes ... diagnosis #management #hepatology ... #gastroenterology
Differentiation Syndrome in APML Epidemiology: • Incidence: common in APL (2-48% depending on the study) • Triggers:
ATRA treatment Pathophysiology ... Diagnosis: >3 symptoms ... or> 1 with no other ... Timing, generally either ... diagnosis #management #hematology
Chronic Lymphocytic Leukemia - Summary Cancer affecting lymphocytes/Mature B cell neoplasm • Lymphocytes accumulate in large numbers
with no early symptoms ... classical CLL and other ... kinase (BTK) Complications ... leukemia • GI complications ... workup #oncology #hematology
The 6 C’s of Primary Sclerosing Cholangitis (PSC) PSC is a chronic, cholestatic, immune-mediated disease characterized by
CHOLANGITIS - Genetic ... Care focuses on symptom ... Other approaches ... management #summary #Hepatology
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