Rare genetic disease and the diagnostic odyssey: a caregiver’s journey

BulletArticle
共享以下内容:
IMG_5398

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.

共享以下内容:

有关同一主题的更多信息

推荐主题

SequencingRED 2020Rare Diseases
下次阅读
Scroll to Top