Ask About Aarskog Podcast Series
Lisa Hume
The Aarskog Foundation is the world’s only patient and parent-led organisation for the X-linked rare genetic condition Aarskog Syndrome. Our Ask About Aarskog campaign seeks to raise awareness around the importance of early diagnosis for children and raise funds towards vital research critical to their future development, health and education. Listen to our podcasts to hear from patients, parents and carriers of Aarskog Syndrome.
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