Drugs that suppress TSH or cause central hypothyroidism
نویسندگان
چکیده
منابع مشابه
Drugs That May Cause or Exacerbate Heart Failure
August 9, 2016 Circulation. 2016;134:e32–e69. DOI: 10.1161/CIR.0000000000000426 e32 Robert L. Page II, PharmD, MSPH, FAHA, Chair Cindy L. O’Bryant, PharmD Davy Cheng, MD, MSc Tristan J. Dow, MD Bonnie Ky, MD, MSCE C. Michael Stein, MB ChB, FAHA Anne P. Spencer, PharmD Robin J. Trupp, PhD, ACNP-BC, FAHA JoAnn Lindenfeld, MD, FAHA, Co-Chair On behalf of the American Heart Association Clinical Pha...
متن کاملRaised serum TSH in hypothyroidism.
It is desirable to detect early hypothyroidism of the mildest degree even before conventional tests of thyroid function become abnormal. Serum TSH levels (normal: undetectable to 4 muU/ml) rise in patients with mild hypothyroidism long before serum T4 and T3 levels fall. In the patient described the serum TSH level was 310 muU/ml, while other tests of thyroid function gave normal results. After...
متن کاملHypothyroidism and obesity. Cause or effect?
OBJECTIVE To establish relationship between obesity and hypothyroidism and to analyze the frequency the frequency of primary hypothyroidism in obese patients and frequency of obesity in primary hypothyroidism patients. METHODS We conducted this retrospective, observational study in the Department of Endocrinology and Obesity Clinic, Medwin Hospital, Hyderabad, India in Mar 2008. In the last 1...
متن کاملNeonatal screening and a new cause of congenital central hypothyroidism
Congenital central hypothyroidism (C-CH) is a rare disease in which thyroid hormone deficiency is caused by insufficient thyrotropin (TSH) stimulation of a normally-located thyroid gland. Most patients with C-CH have low free thyroxine levels and inappropriately low or normal TSH levels, although a few have slightly elevated TSH levels. Autosomal recessive TSH deficiency and thyrotropin-releasi...
متن کاملA boy with low-TSH hypothyroidism.
A case of long-standing mild hypothyroidism is described. This was caused by partial TSH deficiency probably of hypothalamic origin, with no other pituitary hormone deficiencies, although with a decreased response of FSH and LH to LHRH.
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ژورنال
عنوان ژورنال: Best Practice & Research Clinical Endocrinology & Metabolism
سال: 2009
ISSN: 1521-690X
DOI: 10.1016/j.beem.2009.08.003