Turner Syndrome practice guidelines

Leah Doherty, David M. Brown, Michael Ainslie, Erica Eugster, Betsy Hirsch, Clifford Kashtan, Antoinette Moran, Theodore Nagel, Kumud Sane, Krishna Saxena, Kevin Sheridan, Joseph Sockalosky, Martha Spencer, C. Gail Summers, Christine Ternard

Research output: Contribution to journalReview article

Abstract

Turner Syndrome (TS) consists of short stature, a spectrum of karyotypes and abnormalities of the ovaries, heart, and kidneys, and changes in the eyes and ears. Reproductive problems, learning disabilities, and psychosocial issues may further compound the care of children and women with TS. TS requires lifelong, multispecialty integrated care and guidance and involvement of the patient and parents with ongoing education and support.

Original languageEnglish (US)
Pages (from-to)443-447
Number of pages5
JournalEndocrinologist
Volume7
Issue number6
DOIs
StatePublished - Dec 1997

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ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism

Cite this

Doherty, L., Brown, D. M., Ainslie, M., Eugster, E., Hirsch, B., Kashtan, C., Moran, A., Nagel, T., Sane, K., Saxena, K., Sheridan, K., Sockalosky, J., Spencer, M., Summers, C. G., & Ternard, C. (1997). Turner Syndrome practice guidelines. Endocrinologist, 7(6), 443-447. https://doi.org/10.1097/00019616-199707060-00006