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
Ноябрь 16, 2022
Статья

Получите подписку на последние новости и обновления LabInsights

Подпишитесь на рассылку Lab Insights и получайте последние новости и обновления

Другие материалы по этой же теме
Select a related post from the options below.
Читать далее