6 results
symptoms cushings dementia differential endocrinology genetics geriatrics hematology hemeonc hemophagocytic hepatology hepatorenal hlh hrs hypercortisolism lymphohistiocytosis management nephrology pediatrics peds
Major neurocognitive disorders (MNCD): Diagnosis and workup 1) Clinical diagnosis Cognitive impairment + loss of autonomy 2)
workup 1) Clinical ... workup What type ... Aphaso-apraxo-agnosia syndrome ... (parkinsonian signs ... Differential #Subtypes #Classification
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... Pathogenesis and clinical ... Syndrome Signs ... • Obesity -> Type ... #genetics #pathophysiology
Cushing's Syndrome - Hypercortisolism - Diagnosis and Clinical Features 1) Skin • Thin, easily bruisable skin with
Cushing's Syndrome ... Hypercortisolism - Diagnosis ... and Clinical Features ... dehydrogenase type ... #signs #symptoms
Serotonin Syndrome: Pathogenesis and Clinical Findings Serotonin Syndrome: Variable combination of mental status changes, autonomic instability, and
Serotonin Syndrome ... diagnosis - History ... #Pathophysiology ... #Psychiatry #Diagnosis ... #Signs #Symptoms
Hepatorenal Syndrome (HRS) Definition: • Functional, potentially reversible kidney impairment. • Occurs in advanced liver disease: cirrhosis, severe alcoholic
Hepatorenal Syndrome ... Pathophysiology: ... Diagnosis (Clinical ... Classification: ... HRS-AKI (formerly Type
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
HLH is a critical ... Types of HLH • ... Clinical Presentation ... • Common Signs ... Pathophysiology
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