Smart software revolutionizing how medicine is practiced.
Recap of CT’s event and interviews with Angelman Syndrome and ALD patient advocates
Discuss red flags for inherited cardiovascular disease, genetic cascade screening, prevention/risk reduction and notifying at-risk relatives of patients.
Rare Disease advocate and caregiver shares on the resources she has created.
Patient Advocate shares his pre-symptomatically genetically diagnosis and the latest breakthrough in research
Discuss classification of genetic variants including Variants of Unknown Significance (VUS)
A member of Sarah Lawrence’s genetic counseling admission committee offers advice for applicants.
Patient advocate shares about her two rare brain tumors and hereditary cancer syndrome.
Daniel speaks about the films to be screened at the festival and the film he produced about his son's rare disease, Menkes Disease.