In December 2021, Arihai Greene was born with signs of Prader-Willi syndrome (PWS), a rare and serious genetic disorder that includes a complex spectrum of cognitive, behavioural and developmental problems. In this session, his father will discuss the diagnostic odyssey, including the emotional experience of navigating the Singapore healthcare system and coping with a PWS diagnosis. He will also highlight opportunities for healthcare professionals to improve the patient experience in rare disease diagnostics and clinical care.
Rare genetic disease and the diagnostic odyssey: a caregiver’s journey
訂閱 LabInsights 最新新聞和更新
更多相同主題
訂閱 LabInsights 最新新聞和更新
接下來讀取
- C-Suite Perspectives, Event Coverage, Healthcare Transformation, Management, RED 2024
- C-Suite Perspectives, Leaders In Conversation, Management
- Healthcare Transformation, Management, Operations, Population Health Management
- Disease Area, Healthcare Transformation, Histopathology, Leaders In Conversation, Management, Oncology, Operations