Tiroid hormone direnci: nadir bir sendrom
Journal Title: Dicle Tıp Dergisi - Year 2011, Vol 38, Issue 3
Abstract
Tiroid hormon direnci sendromu (RTH) genellikle otozomal dominant kalitim gösteren nadir bir hastalıktır. Tiroid hormon direnci olan hastalar genellikle ötiroid olurlar fakat nadir de olsa tirotoksikoz veya hipotiroidizm belirti ve bulguları ile seyredilebilir. Biz bu yazıda ilginç bir sendrom olarak tiroid hormon direnci olan fakat aile öyküsü olmayan bir olgu sunulmaktadır. Olgumuzda yüksek serum tiroid hormon düzeyleri ve normal TSH düzeylerine rağmen guatr, kilo alımında artış ve normal zeka durumu gözlendi
Authors and Affiliations
Yunus Kibar, Şenay Arıkan, Ayşe Çarlıoğlu, Yasin Öztürk, Ahmet Tay, Mehmet Ayhan
Keywords
Related Articles
- EP ID EP97479
- DOI -
- Views 133
- Downloads 0
The effectiveness of single port thoracoscopic approach in pleural effusions
Objective: Currently, thoracoscopic procedures have been used frequently in diagnosis and treatment of pleural effusions. It was reported, high diagnosis and treatment success with thoracoscopy in pleural effusion, whic...
Videoflorografide saptanan bir özofagorespiratuar fistül olgusu
Bu olgu bildirisinde, yemek sırasında tekrarlayan öksürme ve boğulma nöbetleri olan 59 yaşında bir kadın hasta sunulmuştur. Geçmişinde, mediastinal lenf bezlerinde metastatik tümör bulunması nedeniyle radyasyon ve kem...
Adenosine Deaminase Gene G22a Polymorphism as a Risk Factor for Schizophrenia in Turkish Population
Objective: The aim of this study was to investigate whether the G22A polymorphism of adenosine deaminase (ADA) gene is associated with schizophrenia in Turkish population. Methods: In this study, we evaluated 113 pati...
The protective effects of omega-3 fatty acids on rat testicular tissue
Objectives: In this study, the protective effect of omega-3 fatty acids on testicular tissue was aimed to investigate at biochemical levels. Materials and methods: Totally, 16 adult male Wistar rats were divided into tw...
Primary hyperoxaluria with development of renal failure during infancy: Report of two cases
Primary hyperoxaluria is a rare genetic disorder in glyoxylate metabolism that leads to systemic overproduction of oxalate. The disorder results in overproduction and excessive urinary excretion of oxalate, causing re...