先天性甲状腺機能亢進症
WordNet
- an overactive thyroid gland; pathologically excessive production of thyroid hormones or the condition resulting from excessive production of thyroid hormones (同)thyrotoxicosis
- present at birth but not necessarily hereditary; acquired during fetal development (同)inborn, innate
PrepTutorEJDIC
- 甲状腺機能高進症(バセドウ病,神経過敏症などを起こす)
- (病気・身体的欠陥など)生まれつきの,先天的な
UpToDate Contents
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English Journal
- Maternal manifestation of Ballantyne's syndrome occurring concomitantly with the development of fetal congenital mesoblastic nephroma.
- Takahashi H1, Matsubara S, Kuwata T, Ohkuchi A, Mukoda Y, Saito K, Usui R, Suzuki M.
- The journal of obstetrics and gynaecology research.J Obstet Gynaecol Res.2014 Apr;40(4):1114-7. doi: 10.1111/jog.12286. Epub 2014 Jan 15.
- Various fetal or placental disorders cause Ballantyne's (mirror) syndrome. For the first time, we report a maternal manifestation of Ballantyne's syndrome occurring concomitantly with the development of fetal congenital mesoblastic nephroma (CMN). In a pregnant woman with a CMN fetus, lung edema, hy
- PMID 24428571
- Highlights in thyroidology: a historical vignette.
- Weissel M.
- Wiener klinische Wochenschrift.Wien Klin Wochenschr.2014 Mar 21. [Epub ahead of print]
- This review gives a historical overview about the development of today's understanding of benign thyroid diseases and the possibilities of their treatment.Little was known about the thyroid gland until the nineteenth century: the state of knowledge was (1) that something in food, especially in seawe
- PMID 24652010
- A 20-year experience in microsurgical treatment of choanal atresia.
- Rodríguez H1, Cuestas G2, Passali D1.
- Acta otorrinolaringológica española.Acta Otorrinolaringol Esp.2014 Mar-Apr;65(2):85-92. doi: 10.1016/j.otorri.2013.09.005. Epub 2014 Feb 17.
- INTRODUCTION AND OBJECTIVES: Choanal atresia is the most common congenital nasal anomaly. Diagnosis is confirmed by endoscopic examination and computed tomography. The definitive treatment is surgical, and different surgical techniques and approaches are used. We describe our experience in transnasa
- PMID 24556158
Japanese Journal
- Left Main Coronary Artery Compression Syndrome with an Incomplete Atrioventricular Septal Defect Presenting as Angina Induced by Hyperthyroidism
- 小児科関連の甲状腺疾患の遺伝子変異 (特集 小児科領域の甲状腺疾患・甲状腺関連遺伝子変異)
- Combined treatment with bicalutamide and anastrozole in a young boy with peripheral precocious puberty due to McCune-Albright Syndrome
Related Links
- 1. Exp Clin Endocrinol Diabetes. 1997;105 Suppl 4:6-11. Congenital hyperthyroidism. Krude H, Biebermann H, Krohn HP, Dralle H, Grüters A. Congenital hyperthyroidism is a very rare disease. But, for each affected child it has to be ...
- Original Article Brief Report Congenital Hyperthyroidism Caused by a Mutation in the Thyrotropin-Receptor Gene Peter Kopp, M.D., Jacqueline van Sande, M.D., Jasmine Parma, M.D., Laurence Duprez, M.D., Hans ...
Related Pictures
★リンクテーブル★
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- 関
- congenital、congenitally
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甲状腺機能亢進症