𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Evidence for Genetic Heterogeneity of the Carney Complex (Familial Atrial Myxoma Syndromes)

✍ Scribed by Jeff Milunsky; Xin-Li Huang; Clinton T Baldwin; Michel G Farah; Aubrey Milunsky


Book ID
114136782
Publisher
Elsevier Science
Year
1998
Tongue
English
Weight
143 KB
Volume
106
Category
Article
ISSN
0165-4608

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Molecular genetic diagnosis of the famil
✍ Goldstein, Marsha M.; Casey, Mairead; Carney, J. Aidan; Basson, Craig T. πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 18 KB πŸ‘ 2 views

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

Genetic testing of the family with a Car
✍ Nicholas Aspres; Narelle R Bleasel; Karen M Stapleton πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 41 KB

## Summary Carney complex is a rare cardiocutaneous syndrome with an autosomal‐dominant inheritance pattern. Apart from its cutaneous manifestations of multiple blue naevi and lentigines, it can involve multiple other organ systems, particularly the heart, where myxoma tumours commonly develop and

Further evidence for genetic heterogenei
✍ Wang, Tso-Ren ;Lin, Shio-Jean ;Opitz, John M. ;Reynolds, James F. πŸ“‚ Article πŸ“… 1987 πŸ› John Wiley and Sons 🌐 English βš– 266 KB πŸ‘ 2 views

We report on 2 brothers with severe manifestations of the whistling-face/windmill-vane-hand syndrome (also called "craniocarpotarsal dystrophy"; Freeman-Sheldon syndrome); they were born to normal, nonconsanguineous parents. Our observations support the theory of causal heterogeneity of this syndrom