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Autor:
Janet Thomas MD, Mina Nguyen-Driver PsyD, Heather Bausell RD, LDN, Jane Breck MD, Javier Zambrano MD, Vanessa Birardi PharmD
Publikováno v:
Journal of Inborn Errors of Metabolism and Screening, Vol 5 (2017)
Nearly half of all patients diagnosed with phenylalanine hydroxylase (PAH) deficiency, also known as phenylketonuria, are lost to follow-up (LTFU); most are adults who stopped attending clinic after the age of 18 years. To understand why adult patien
Externí odkaz:
https://doaj.org/article/63631d3eed86453ca417181d4908b9ec
