Turner Syndrome

Marsha L. Davenport; Judith Ross; Phillippe F. Backeljauw

doi:10.1007/978-1-60761-395-4_7

Turner Syndrome

Marsha L. Davenport
, Judith Ross
, Phillippe F. Backeljauw

Department of Pediatrics, Delaware Valley

University of North Carolina at Chapel Hill
Thomas Jefferson University
Cincinnati Children's Hospital Medical Center

Producción científica › revisión exhaustiva

Resumen

Turner syndrome (TS) is one of the most common human chromosome anomalies. It occurs in approximately 1:2,000 female live births regardless of ethnic background. Girls with TS have an abnormal or missing X chromosome that causes short stature and may cause lymphedema, cardiac abnormalities, gonadal dysgenesis, dysmorphic features, nonverbal learning disabilities, and other problems.

Idioma original	English
Título de la publicación alojada	Pediatric Endocrinology
Subtítulo de la publicación alojada	A Practical Clinical Guide, Second Edition
Editorial	Humana Press Inc.
Páginas	109-135
Número de páginas	27
ISBN (versión digital)	9781607613954
ISBN (versión impresa)	9781607613947
DOI	https://doi.org/10.1007/978-1-60761-395-4_7
Estado	Published - 1 ene 2013

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10.1007/978-1-60761-395-4_7

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abstract = "Turner syndrome (TS) is one of the most common human chromosome anomalies. It occurs in approximately 1:2,000 female live births regardless of ethnic background. Girls with TS have an abnormal or missing X chromosome that causes short stature and may cause lymphedema, cardiac abnormalities, gonadal dysgenesis, dysmorphic features, nonverbal learning disabilities, and other problems.",

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Turner Syndrome

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