Abstract Turner syndrome affects 25–50 per 100,000 females and can involve multiple
organs through all stages of life, necessitating multidisciplinary approach to care. Previous …

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Abstract Turner syndrome (TS; ORPHA 881) is a rare condition in which all or part of one X
chromosome is absent from some or all cells. It affects approximately one in every 1/2500 …

Turner syndrome is recognized now as a syndrome familiar not only to pediatricians and
pediatric specialists, medical geneticists, adult endocrinologists, and cardiologists, but also …

Background: Turner Syndrome is associated with an increased risk of autoimmune
diseases, such as autoimmune thyroiditis, coeliac disease, type 1 diabetes mellitus …

Turner syndrome (TS) results from a sex-chromosomal anomaly characterized by presence
of one normal X chromosome and the loss of the second X-chromosome in phenotypic …

Turner Syndrome (TS) is a common genetic disorder, affecting female individuals, resulting
from the partial or complete absence of one sex chromosome, and occurring in …

The histopathological diagnosis of melanocytic tumors, including malignant melanoma
(hence referred to as melanoma) and benign melanocytic nevi, has been the subject of …

An increased frequency of autoimmune diseases as well as an elevated incidence of
autoantibodies has been observed in patients with Turner syndrome; the most common …

Abnormal skin pigmentation represents a common skin problem which may be congenitally
determined or acquired during life. The former are discussed in Chapter [70]. Acquired …