نتایج جستجو برای: carney complex

تعداد نتایج: 784155  

Journal: :The Journal of clinical endocrinology and metabolism 2004
Daniel F Gunther Isabelle Bourdeau Ludmila Matyakhina David Cassarino David E Kleiner Kurt Griffin Nickolas Courkoutsakis Mones Abu-Asab Maria Tsokos Meg Keil J Aidan Carney Constantine A Stratakis

Cushing syndrome is uncommon in childhood and rare in infancy. We report the case of a 3-yr-old child who presented with symptoms of Cushing syndrome beginning shortly after birth. Her hypercortisolemia was cyclical, causing relapsing and remitting symptoms, which eventually led to suspicions of possible Munchausen syndrome by proxy. Investigation at the National Institutes of Health excluded e...

Journal: :Cancer research 2005
Lawrence S Kirschner Donna F Kusewitt Ludmila Matyakhina William H Towns J Aidan Carney Heiner Westphal Constantine A Stratakis

Carney complex is an autosomal dominant neoplasia syndrome characterized by spotty skin pigmentation, myxomatosis, endocrine tumors, and schwannomas. This condition may be caused by inactivating mutations in PRKAR1A, the gene encoding the type 1A regulatory subunit of protein kinase A. To better understand the mechanism by which PRKAR1A mutations cause disease, we have developed conventional an...

Journal: :The Journal of pathology 2017
I-Ching Tseng Wei-Ju Huang Yu-Ling Jhuang Ya-Yun Chang Hung-Pin Hsu Yung-Ming Jeng

Cardiac myxoma is the most common cardiac tumour. Most lesions occur sporadically, but occasional lesions develop in patients with Carney complex, a syndrome characterized by cardiac myxoma, spotty pigmentation, and endocrine overactivity. Two-thirds of patients with Carney complex harbour germline mutations in PRKAR1A, which encodes the type I regulatory subunit of protein kinase A (PKA). Most...

2009
Hye-Jong Song Kyoung-Mee Kim Dong Il Choi Cheol Keun Park

Carney triad is a rare syndrome of unknown etiology characterized by having at least two out of three following neoplasms: gastrointestinal stromal tumor, pulmonary chondroma and extra-adrenal paraganglioma. About 100 cases have been reported worldwide. We report a case of Carney triad in a 42-year-old woman presented with a gastrointestinal stromal tumor in the stomach and a malignant function...

Journal: :Oncology reports 2007
Abbas Agaimy Antje-Friederike Pelz Christopher L Corless Peter H Wünsch Michael C Heinrich Ferdinand Hofstaedter Wolfgang Dietmaier Charles D Blanke Peter Wieacker Albert Roessner Arndt Hartmann Regine Schneider-Stock

Carney triad is a rare non-hereditary condition affecting young females and characterized by metachronous or synchronous occurrence of epithelioid gastrointestinal stromal tumours (GISTs), pulmonary chondroma and extra-adrenal paraganglioma. The genetic alterations in Carney triad-related GISTs have not been well studied. We evaluated GISTs from three females with incomplete Carney triad for KI...

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