Homocystinuria patient and caregiver survey: experiences of diagnosis and patient satisfaction.
T MorrisonF BöschM A LandoltV KožichMartina HuemerA A M MorrisPublished in: Orphanet journal of rare diseases (2021)
There is often a long delay in diagnosing the homocystinurias unless this is achieved by newborn screening; this survey also highlights problems with the availability and cost of treatment and the palatability of protein substitutes.