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

BulletArticle
แชร์สิ่งนี้:
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.

แชร์สิ่งนี้:

เพิ่มเติมในหัวข้อเดียวกัน

หัวข้อแนะนำ

การวิเคราะห์หาลำดับRED 2020Rare Diseases
สิ่งที่ต้องอ่านถัดไป
Scroll to Top