Editorial: Carney complex - Clarity and complexity

Journal of Clinical Endocrinology and Metabolism

Volumn 85, Issue 11, 2000, Pages 4010-4011

  Malchoff, Carl D ^a  

^a UNIVERSITY OF CONNECTICUT HEALTH CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CORTICOTROPIN;

ADRENAL CORTEX INSUFFICIENCY; AUTOSOMAL DOMINANT DISORDER; CARNEY COMPLEX; CLINICAL FEATURE; EDITORIAL; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; HUMAN; LEYDIG CELL; PHENOTYPE; PRIORITY JOURNAL; SERTOLI CELL;

FEMALE; GENETIC PREDISPOSITION TO DISEASE; HAMARTOMA SYNDROME, MULTIPLE; HUMANS; MALE; MULTIPLE ENDOCRINE NEOPLASIA; NEOPLASTIC SYNDROMES, HEREDITARY; OVARIAN NEOPLASMS; PIGMENTATION DISORDERS; SYNDROME;

EID: 0034527485     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.85.11.4010     Document Type: Editorial

References (12)

1. The complex of myxomas, spotty pigmentation, and endocrine overactivity
2. Immunoglobulins of patients with Cushing's syndrome due to pigmented adrenocortical micronodular dysplasia stimulate in vitro steroido-genesis
3. Sporadic cardiac myxomas and tumors from patients with Carney complex are not associated with activating mutations of the Gsa gene
4. G protein-coupled receptor structure and function: The impact of disease-causing mutations
5. Activating mutations of the stimulatory G protein in the McCune-Albright syndrome
6. Carney complex, a familial multiple neoplasia and lentiginosis syndrome: Analysis of 11 kindreds and linkage to the short arm of chromosome 2
7. Ovarian lesions in Carney complex: Clinical genetics and possible predisposition to malignancy
8. Thyroid gland abnormalities in patients with the syndrome of spotty skin pigmentation, myxomas, endocrine overactivity, and schwannomas (Carney complex)
9. Paradoxical response to dexamethasone assists with the diagnosis of primary pigmented nodular adrenocortical disease (PPNAD)
10. Identification of a novel genetic locus for familial cardiac myxomas and Carney complex
11. Mutations of the gene encoding the protein kinase A type I-α regulatory subunit in patients with the Carney complex
12. Mutations in the protein kinase A R1α regulatory subunit cause familial cardiac myxomas and Carney complex