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Berger HR, Creech MK, Hannoush Z, et al. A NOVEL MUTATION CAUSING COMPLETE THYROID BINDING GLOBULIN DEFICIENCY (TBG-CD MIA) IN A MALE WITH COEXISTING GRAVES DISEASE. AACE Clin Case Rep. 2017;3(2):e134-e139doi: 10.4158/EP161421.CR.
Berger, H. R., Creech, M. K., Hannoush, Z., Watanabe, Y., Kargi, A., & Weiss, R. E. (2017). A NOVEL MUTATION CAUSING COMPLETE THYROID BINDING GLOBULIN DEFICIENCY (TBG-CD MIA) IN A MALE WITH COEXISTING GRAVES DISEASE. AACE clinical case reports, 3(2), e134-e139. https://doi.org/10.4158/EP161421.CR
Berger, Hara Rosen, et al. "A NOVEL MUTATION CAUSING COMPLETE THYROID BINDING GLOBULIN DEFICIENCY (TBG-CD MIA) IN A MALE WITH COEXISTING GRAVES DISEASE." AACE clinical case reports vol. 3,2 (2017): e134-e139. doi: https://doi.org/10.4158/EP161421.CR
Berger HR, Creech MK, Hannoush Z, Watanabe Y, Kargi A, Weiss RE. A NOVEL MUTATION CAUSING COMPLETE THYROID BINDING GLOBULIN DEFICIENCY (TBG-CD MIA) IN A MALE WITH COEXISTING GRAVES DISEASE. AACE Clin Case Rep. 2017;3(2):e134-e139. doi: 10.4158/EP161421.CR. PMID: 28553659; PMCID: PMC5444812.
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AACE Clin Case Rep. 2017;3(2):e134-e139. doi: 10.4158/EP161421.CR.

A NOVEL MUTATION CAUSING COMPLETE THYROID BINDING GLOBULIN DEFICIENCY (TBG-CD MIA) IN A MALE WITH COEXISTING GRAVES DISEASE.

AACE clinical case reports

Hara Rosen Berger, Matthew K Creech, Zeina Hannoush, Yui Watanabe, Atil Kargi, Roy E Weiss

Affiliations

  1. Department of Medicine, Division of Endocrinology, Diabetes and Metabolism, University of Miami Miller School of Medicine, Miami, FL, United States.
  2. Jackson Health System, Miami, FL, United States.

PMID: 28553659 PMCID: PMC5444812 DOI: 10.4158/EP161421.CR

Abstract

OBJECTIVE: An asymptomatic male was found on screening to have a low serum TSH and total T

METHODS: The laboratory testing included total T

RESULTS: A 35-year-old East Indian male was referred to endocrinology because of abnormal thyroid function tests (TFTs): TSH 0.01 mIU/L (0.4-3.6), total T

CONCLUSION: Patients with Graves' disease harboring a

Keywords: Complete Deficiency; Graves’ disease; TBG; Thyroxine-binding globulin

References

  1. Hum Genet. 1995 Oct;96(4):481-2 - PubMed
  2. Acta Endocrinol (Copenh). 1964 Jan;45:99-113 - PubMed
  3. Endocr Rev. 1989 Aug;10(3):275-93 - PubMed
  4. J Pediatr Endocrinol Metab. 2015 Jan;28(1-2):241-5 - PubMed
  5. J Pediatr. 1993 Feb;122(2):227-30 - PubMed
  6. J Clin Endocrinol Metab. 1961 Nov;21:1455-68 - PubMed
  7. J Pediatr. 1993 Aug;123(2):333-4 - PubMed
  8. Acta Med Scand. 1974 Jan-Feb;195(1-2):5-9 - PubMed
  9. Med Princ Pract. 2008;17(1):61-5 - PubMed
  10. J Clin Endocrinol Metab. 1977 Feb;44(2):242-7 - PubMed
  11. Clin Endocrinol (Oxf). 1981 Sep;15(3):313-8 - PubMed
  12. Nat Rev Endocrinol. 2013 Dec;9(12):724-34 - PubMed
  13. Intern Med. 1995 May;34(5):413-7 - PubMed
  14. J Endocrinol Invest. 1990 Apr;13(4):343-9 - PubMed
  15. Horm Res. 1996;45(3-5):128-38 - PubMed
  16. Best Pract Res Clin Endocrinol Metab. 2015 Oct;29(5):735-47 - PubMed
  17. Endocrinol Jpn. 1992 Dec;39(6):577-84 - PubMed
  18. Arch Intern Med. 1988 Jun;148(6):1445-6 - PubMed
  19. Horm Metab Res. 2014 Feb;46(2):100-8 - PubMed
  20. Jpn J Med. 1986 May;25(2):186-90 - PubMed

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