Turner syndrome (TS), a genetic disorder due to incomplete dosage compensation of X-
linked genes, affects multiple organ systems, leading to hypogonadotropic hypogonadism …

Turner syndrome (TS) is a complex developmental disorder in individuals with short stature
who possess a 45, X cell line, with or without mosaicism. Because the single X chromosome …

Turner syndrome is a rare condition in women that is associated with either complete or
partial loss of one X chromosome, often in mosaic karyotypes. Turner syndrome is …

Abstract In 1938, Dr. Henry H. Turner wrote:“the triad, infantilism, webbing of the neck, and
deformity of the elbow (cubitus valgus), occurring in the same individual is unusual and …

Turner syndrome (TS) is a condition in females missing the second sex chromosome (45, X)
or parts thereof. It is considered a rare genetic condition and is associated with a wide range …

Turner syndrome is a rare disorder resulting from complete or partial loss of the second sex
chromosome. Common manifestations include delayed growth, premature ovarian failure …

Ovarian dysgenesis, short stature, and infertility are common features of Turner syndrome
(TS). Endocrinopathies and cardiopathies are less common, but may induce significant …

Turner syndrome (TS), also known as Congenital ovarian hypoplasia syndrome, occurs
when the X chromosome is partially or completely missing in females. Its main clinical …

Turner syndrome (TS) is a phenotypic heterogeneous genetic disorder caused by the loss of
an X‑chromosome or X‑structural abnormalities in the X‑chromosome, and affects …

Objective To describe in practical terms the clinical management in adult life of patients with
Turner syndrome. Material & methods Systematic review of the literature and practical …