ea0059p083 | Clinical practice, governance & case reports | SFEBES2018
Chan Yin Chun Alex
, Kuo Pei-juo
, Mahmod Sameer
, Levy Miles J
, Reddy Narendra L
, Yusuff Shafiq
, Bhake Ragini C
Background: TS, resulting from partial or complete loss of an X-chromosome, is a rare diagnosis1. In addition to its well-described phenotypic features2, a number of multi-systemic conditions may develop over the lifespan of a Turner female that require long-term surveillance which is challenging to deliver in todays specialised services NHS.Aim: To evaluate UHL service provision against the only guidelines for the...