نتایج جستجو برای: prkar1a protein

تعداد نتایج: 1234776  

2017
Qiuli Liu Dali Tong Gaolei Liu Yuting Yi Dianzheng Zhang Jun Zhang Yao Zhang Zaoming Huang Yaoming Li Rongrong Chen Yanfang Guan Xin Yi Jun Jiang

RATIONALE Carney complex (CNC) is a multiple neoplasia syndrome with autosomal dominant inheritance. CNC is characterized by the presence of myxomas, spotty skin pigmentation, and endocrine overactivity. No direct correlation has been established between disease-causing mutations and phenotype. PATIENT CONCERNS A 16-year-old boy was admitted because of excessive weight gain over 3 years and p...

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...

Journal: :The Journal of clinical endocrinology and metabolism 2001
C A Stratakis L S Kirschner J A Carney

Carney complex is a multiple neoplasia syndrome featuring cardiac, endocrine, cutaneous, and neural tumors, as well as a variety of pigmented lesions of the skin and mucosae. Carney complex is inherited as an autosomal dominant trait and may simultaneously involve multiple endocrine glands, as in the classic multiple endocrine neoplasia syndromes 1 and 2. Carney complex also has some similariti...

Journal: :Schizophrenia research 2016
Diego A Forero Liesbet Herteleer Sonia De Zutter Karl-Fredrik Norrback Lars-Göran Nilsson Rolf Adolfsson Patrick Callaerts Jurgen Del-Favero

Identification of novel candidate genes for schizophrenia (SZ) and bipolar disorder (BP), two psychiatric disorders with large epidemiological impacts, is a key research area in neurosciences and psychiatric genetics. Previous evidence from genome-wide studies suggests an important role for genes involved in synaptic plasticity in the risk for SZ and BP. We used a convergent genomics approach, ...

2012
Ko Un Park Hyun-Sook Kim Seung Kwan Lee Woon-Won Jung Yong-Koo Park

A case of Carney complex in a Korean patient is presented. The patient had the characteristics of Carney complex including skin lesions, positive family history, and multiple myxomas including a superficial angiomyxoma in the perianal area. An extensive genetic analysis revealed a novel mutation in the protein kinase A type I-a regulatory subunit (PRKAR1A) gene, but not in the phosphodiesterase...

2010
Isabelle Sahut-Barnola Cyrille de Joussineau Pierre Val Sarah Lambert-Langlais Christelle Damon Anne-Marie Lefrançois-Martinez Jean-Christophe Pointud Geoffroy Marceau Vincent Sapin Frédérique Tissier Bruno Ragazzon Jérôme Bertherat Lawrence S. Kirschner Constantine A. Stratakis Antoine Martinez

Carney complex (CNC) is an inherited neoplasia syndrome with endocrine overactivity. Its most frequent endocrine manifestation is primary pigmented nodular adrenocortical disease (PPNAD), a bilateral adrenocortical hyperplasia causing pituitary-independent Cushing's syndrome. Inactivating mutations in PRKAR1A, a gene encoding the type 1 alpha-regulatory subunit (R1alpha) of the cAMP-dependent p...

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