1 / 1
|
DeCS
|
|
|
Descriptor English:
|
|
Carney Complex
|
Descriptor Spanish:
|
|
Complejo de Carney
|
Descriptor Portuguese:
|
|
Complexo de Carney
|
Synonyms English:
|
|
Carney Complex, Type 2
Carney Complex, Type II
Carney Myxoma-Endocrine Complex
Carney Syndrome
LAMB Syndrome
Myxoma, Spotty Pigmentation, and Endocrine Overactivity
NAME Syndrome
|
Tree Number:
|
|
C04.557.450.565.550.312
C04.588.894.309.500
C14.280.459.500
C16.131.077.229
C16.131.831.108
|
Definition English:
|
|
Autosomal dominant syndrome characterized by cardiac and cutaneous MYXOMAS; LENTIGINOSIS (spotty pigmentation of the skin), and endocrinopathy and its associated endocrine tumors. The cardiac myxomas may lead to SUDDEN CARDIAC DEATH and other complications in Carney complex patients. The gene coding for the PRKAR1A protein is one of the causative genetic loci (type 1). A second locus is at chromosome 2p16 (type 2). |
History Note English:
|
|
2010
|
Allowable Qualifiers English:
|
|
|
Record Number:
|
|
53487
|
Unique Identifier:
|
|
D056733
|
Occurrence in VHL:
|
|
|
Similar:
|
|
DeCS CID-10 SciELO LILACS LIS
|