hrp0089p2-p242 | Growth & Syndromes P2 | ESPE2018
Akulevich Natallia
, Makarava Yulia
, Ershova Larissa
, Kunavitch Irina
Turner syndrome (TS) is characterized by partly or completely missing of an X chromosome and variability of clinical signs. We present tree Caucasian mosaic TS girls with unusual clinical course and discuss some literature.Case 1: A girl referred first to paediatric endocrinologist at the age of 8.5 y. for metabolic problems (an excessive weight gain, acanthosis nigricans, impaired glucose tolerance, hyperinsulinemia). The height was not a concern (Media...