Squamosal Suture Craniosynostosis Due to Hyperthyroidism Caused by an Activating Thyrotropin Receptor Mutation (T632I)-Reference-Cited by-同舟云学术

Squamosal Suture Craniosynostosis Due to Hyperthyroidism Caused by an Activating Thyrotropin Receptor Mutation (T632I)

Published:2015-10 Issue:10 Volume:25 Page:1167-1172
ISSN:1050-7256
Container-title:Thyroid
language:en
Short-container-title:Thyroid

Author:

Chawla Reeti¹,Alden Tord D.²,Bizhanova Aigerim³,Kadakia Rachel⁴,Brickman Wendy⁴,Kopp Peter A.⁵

Affiliation:

1. Division of Pediatric Endocrinology, Phoenix Children's Hospital, Phoenix, Arizona.

2. Division of Neurosurgery, Ann and Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, Illinois.

3. Department of Biology, Harold Washington College, Chicago, Illinois.

4. Division of Pediatric Endocrinology, Ann and Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, Illinois.

5. Division of Endocrinology Metabolism and Molecular Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois.

Publisher

Mary Ann Liebert Inc

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

https://www.liebertpub.com/doi/pdf/10.1089/thy.2014.0503

Reference24 articles.

1. Congenital Hyperthyroidism Caused by a Mutation in the Thyrotropin-Receptor Gene

2. Germline mutations in the thyrotropin receptor gene cause non–autoimmune autosomal dominant hyperthyroidism

3. Congenital hyperthyroidism caused by a solitary toxic adenoma harboring a novel somatic mutation (serine281-->isoleucine) in the extracellular domain of the thyrotropin receptor.

4. Genetics and phenomics of inherited and sporadic non-autoimmune hyperthyroidism

5. Expanding clinical spectrum of non-autoimmune hyperthyroidism due to an activating germline mutation, p.M453T, in the thyrotropin receptor gene

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