We describe an individual in whom molecular genetic testing provided a diagnosis of the Carney complex, an autosomal dominant syndrome comprising cutaneous and cardiac myxomas, spotty pigmentation of the skin, and endocrinopathy. Recently, we localized the Carney complex disease gene to chromosome r
Carney complex: Diagnosis and management of the complex of spotty skin pigmentation, myxomas, endocrine overactivity, and schwannomas
β Scribed by Stratakis, Constantine A.; Kirschner, Lawrence S.; Carney, J. Aidan
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 5 KB
- Volume
- 80
- Category
- Article
- ISSN
- 0148-7299
- DOI
- 10.1002/(sici)1096-8628(19981102)80:2<183::aid-ajmg19>3.0.co;2-i
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