33 results
diagnosis management signs hematology peds syndrome cirrhosis treatment cholangitis comparison differential endocrinology findings hemophagocytic hepatopulmonary hlh liverfailure lymphohistiocytosis oncology physicalexam
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Syndrome Signs/Symptoms ... > Neonatal and infantile ... #pathophysiology ... #peds #pediatrics
Cirrhosis leading to Chronic Liver Failure - Clinical Signs and Symptoms #Cirrhosis #LiverFailure #Signs #Symptoms #PhysicalExam #Findings
leading to Chronic Liver ... Failure - Clinical ... Signs and Symptoms ... LiverFailure #Signs #Symptoms ... Findings #Diagnosis #Hepatology
Acute Fatty Liver of Pregnancy (AFLP) Pathophysiology: • Defect in fetal free fatty acid metabolism products →
Pregnancy (AFLP) Pathophysiology ... postpartum): • Initial symptoms ... Maternal Support - Critical ... #Pregnancy #hepatology ... diagnosis #management #pathophysiology
Complications of Measles: Pathogenesis and Clinical Findings • ADEM -> Fever, headache, neck stiffness, BBD, mental
Pathogenesis and Clinical ... N/V, elevated liver ... diagnosis #signs #symptoms ... #pathophysiology
Pediatric Parasomnias and Nightmares: Pathogenesis and clinical findings Parasomnias - Micro-arousal episodes during SWS -> Intense activation of
Pediatric Parasomnias ... Pathogenesis and clinical ... Parasomnias #Nightmares #Pediatrics ... #Peds #pathophysiology ... #symptoms #pharmacology
Hemophagocytic Lymphohistiocytosis (HLH) Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
: Overwhelming clinical ... an underlying genetic ... HLH signs and symptoms ... Diagnosis via genetic ... lymph node, or liver
Abnormal liver function tests algorithm. This figure details the initial response to abnormal liver blood tests.
evaluation of the clinical ... /or suspicious clinical ... symptoms/signs ... the remainder, a clinical ... Abnormal #Algorithm #Hepatology
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
Clinical features of Liver Disease in Children #Cirrhosis #LiverFailure #Signs #Symptoms #PhysicalExam #Findings #Diagnosis #Peds #Pediatrics #Hepatology **
Clinical features ... of Liver Disease ... LiverFailure #Signs #Symptoms ... Diagnosis #Peds #Pediatrics ... #Hepatology
The 6 C’s of Primary Sclerosing Cholangitis (PSC) PSC is a chronic, cholestatic, immune-mediated disease characterized by
CHOLANGITIS - Genetic ... indications for liver ... Care focuses on symptom ... remain subject to clinical ... management #summary #Hepatology
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