Turner Syndrome

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Top Contributors - Khloud Shreif and Lucinda hampton

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Introduction

It is a genetic condition that happens only in females when the sex chromosomes are missing causing medical and developmental problems such as; short height, failure of the ovaries to develop, and heart defects.

Turner syndrome can be diagnosed before birth, or during infancy.  However, the diagnosis can be delayed in girls with mild signs and symptoms until early adulthood.

Mechanism of Injury / Pathological Process

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Clinical Presentation

There is variety in the severity of signs and symptoms among females. In some girls with turner syndrome, the symptoms may not be clear, while in others, several physical features start early. Signs and symptoms may be developing slowly over time, or significant, such as heart defects.

Signs and symptoms at birth or during infancy may include:

Signs and symptoms in childhood, teens, and adulthood

Diagnostic Procedures

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Outcome Measures

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Management / Interventions

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Differential Diagnosis

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Resources

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