Turner's syndrome, the most common chromosome abnormality in females, is th
e consequence of complete absence or partial deletion of one X chromosome.
It is associated with a wide spectrum of clinical features of which short s
tature and gonadal dysgenesis are almost invariably present. Women with Tur
ner's syndrome have a reduced life expectancy primarily as a result of card
iovascular disease. They are also susceptible to a number of other disorder
s including autoimmune thyroiditis, osteoporosis, renal and gastrointestina
l disease. Thus, women with Turner's syndrome should be followed up by a mu
ltidisciplinary team of physicians with an interest in the disorder followi
ng discharge from paediatric care. This review aims to highlight the proble
ms associated with Turner's syndrome in adulthood and to discuss important
management strategies.