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dementia diagnosis genetics mncd pediatrics praderwilli workup
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Signs/Symptoms ... • Obesity -> Type ... #genetics #pathophysiology ... #peds #pediatrics
Major neurocognitive disorders (MNCD): Diagnosis and workup 1) Clinical diagnosis Cognitive impairment + loss of autonomy 2)
workup 1) Clinical ... diagnostic workup What type ... Aphaso-apraxo-agnosia syndrome ... (parkinsonian signs ... #Subtypes #Classification
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