Turner Syndrome (TS) is a rare genetic disorder that affects females when one of the X
chromosomes is partially or completely missing. Due to high genetic and phenotypic …

Turner syndrome (TS) was first reported in the literature in 1938 by Laurel Thatcher Ulrich
and Henry Turner. This chromosomal alteration only affects female individuals, who have …

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The overall aim of this thesis was to study dentofacial morphology in Turner syndrome (TS)
versus controls and the influence hereupon from karyotype. One hundred thirty two TS …

The spectrum of Turner syndrome (TS) includes Turner syndrome mosaicism (TSM), which
is typically a nonhereditary chromosomal abnormality. Turner syndrome mosaicism presents …

Objective: The objective of the present study was to describe the phenotypic features of
Turner syndrome (TS) and to investigate the relationship between the genotype and the …

Turner syndrome is a sex chromosome abnormality in which a female has a single X
chromosome or structurally deficient second sex chromosome. The phenotypic spectrum is …

Background Turner syndrome (TS) is a common genetic disorder caused by abnormalities of
the X chromosome. We aimed to describe the phenotypic characteristics of TS patients and …

OBJECTIVE: To identify and characterize otolaryngologic markers for the early diagnosis of
Turner syndrome (TS). STUDY DESIGN: Prospective cohort survey. METHODS: Setting …

Introduction: A complete or partial absence of an X chromosome in the karyotype of
phenotypic females has an impact on craniofacial morphology. The aim of this study was to …