3 results
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Signs/Symptoms ... fractures • Short ... • Obesity -> Type ... pulmonale #PraderWilli ... #Syndrome #genetics
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 ... hyperorality, - 25% genetic
This is a suprasternal notch view demonstrating an aortic flap in a patient with a Stanford
with suspicious signs ... /symptoms allows ... for a more rapid diagnosis ... Delta Hospital #Clinical ... SuprasternalNotch #AorticFlap #Aorta