نتایج جستجو برای: carney complex

تعداد نتایج: 784155  

2011
Young Mi Kang Yoon Hee Kim

Carney complex is an autosomal dominant disorder that occurs due to a mutation in PRKAR1A, which encodes protein kinase A. The clinical features are multiple endocrine gland neoplasms, skin tumors, pigmented skin lesions, myxomas, and schwannomas. In Carney complex, the cardiac myxoma is a common co-morbidity. It occurs in multiples, during young age, regardless of gender and cardiac chamber an...

2013
Vaibhav Pandey Vivek Srivastava Anand kumar Mumtaz Ansari S. K. Singh

Primary pigmented nodular adrenocortical disease (PPNAD) is a rare cause of familial Cushing's syndrome. It is characterized by bilateral adrenocortical hyperplasia with small to normal-sized adrenal glands containing multiple small adrenal cortical pigmented nodules [1,2]. PPNAD may occur in an isolated form or as familial PPNAD. Familial cases of PPNAD are usually associated with Carney compl...

2015
Hongwei Guo Jianping Xu Hui Xiong Shengshou Hu

Carney complex is an autosomal dominant disease that is clinically characterized by cardiac myxomas, spotty skin pigmentation, and endocrine overactivity. Carney complex is most commonly caused by mutations in the PRKAR1A gene on chromosome 17q22-24. Currently, there are at least 117 pathogenic mutations in PRKAR1A that have been identified. Herein, we report on two cases of Carney complex in r...

2008
Jozef Novák-Marcinčin

Group technology (GT) has a great significance in the engineering industry. There is the greatest utilisation of GT in planning activities, especially in process planning and in layout machine design. GT is a manufacturing philosophy that has proved successful by grouping parts into families to speed production and reduce costs. In addition, the application of GT can lead to reductions of in-pr...

امین الرعایا, اشرف, امینی, مسعود, رضوانیان, حسن, طاهری, دیانا, طلایی, افسانه, مهدوی, کیانوری,

سندرم کارنی (Carney Complex) یک سندرم اتوزومال غالب است که با تومورهای مختلف شامل میکزوما در محل‌های متفاوت، تومورهای اندوکرین و ضایعه‌های لنتیگو مشخص می‌شود و تاکنون در ایران گزارش نشده است. بیماری که دراین مقاله معرفی می‌شود، زن 27 ساله‌ای است که با علایم درد پهلو، مراجعه کرده بود. در معاینه با توجه به علایم هیرسوتیسم، چاقی تنه‌ای، هیپرپیگمانتاسیون و هیپرتانسیون، سندرم کوشینگ مطرح شد و با آزم...

Journal: :Korean Journal of Pathology 2012

Journal: :Orphanet Journal of Rare Diseases 2006
Jérôme Bertherat

The Carney complex (CNC) is a dominantly inherited syndrome characterized by spotty skin pigmentation, endocrine overactivity and myxomas. Skin pigmentation anomalies include lentigines and blue naevi. The most common endocrine gland manifestations are acromegaly, thyroid and testicular tumors, and adrenocorticotropic hormone (ACTH)-independent Cushing's syndrome due to primary pigmented nodula...

Journal: :Journal of Cardiothoracic and Vascular Anesthesia 2018

Journal: :Endocrine Abstracts 2015

Journal: :American Journal of Surgical Pathology 2017

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