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Case Reports in Pediatrics
Volume 2011 (2011), Article ID 369871, 4 pages
http://dx.doi.org/10.1155/2011/369871
Case Report

Congenital Central Hypothyroidism due to a Homozygous Mutation in the TSHβ Subunit Gene

1Center for Pediatrics and Adolescent Medicine, University Hospital Freiburg, 79106 Freiburg, Germany
2Department of Pediatrics, Johannes Gutenberg University Medical School, Mainz, Germany
3Department of Pediatric Pulmonology, Clinic for Pediatric and Adolescent Medicine, University Lübeck, Lübeck, Germany
4Department of Radiology, St. Josefskrankenhaus Heidelberg, Freiburg, Germany

Received 9 September 2011; Accepted 4 October 2011

Academic Editor: F.-S. Lo

Copyright © 2011 Sarah Catharina Grünert et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

Sarah Catharina Grünert, Miriam Schmidts, Joachim Pohlenz, Matthias Volkmar Kopp, Markus Uhl, and Karl Otfried Schwab, “Congenital Central Hypothyroidism due to a Homozygous Mutation in the TSHβ Subunit Gene,” Case Reports in Pediatrics, vol. 2011, Article ID 369871, 4 pages, 2011. doi:10.1155/2011/369871