AbstractLEOPARD syndrome, one of many cardiocutaneous syndromes, is an acronym for some of the obvious manifestations of the disease, such as lentigines or ocular hypertelorism. The synonymous name progressive cardiomyopathic lentiginosis better indicates the morbid cardiac features that patients with the syndrome have. A patient with LEOPARD syndrome is presented. He had recurrent upper extremity aneurysms requiring multiple operations and finally PTFE reinforced venous grafts to prevent further aneurysmal degeneration. He has multiple other peripheral aneurysms, thus far asymptomatic. His diagnosis of LEOPARD syndrome was confirmed on a genetic basis. Review of the literature reveals no previous preports of severe aneurysmal disease in th...
The LEOPARD syndrome is a rare, autosomal dominant multisystemic disorder characterized by lentigino...
Leopard Syndrome is a extremely rare disease, autosomal dominant, characterized from a series of sys...
LEOPARD syndrome, also known as Gorlin syndrome II, cardiocutaneous syndrome, lentiginosis profusa s...
is an autosomal dominant multiple congenital anom-aly syndrome, with high penetrance and markedly va...
Abstract LEOPARD syndrome (OMIM #151,100) caused by a germline PTPN11 mutation are characterized as ...
AbstractLEOPARD syndrome is a phenotypic expression of mutations in several genes: PTPN11, RAF1, and...
The L.E.O.P.A.R.D. syndrome is an autosomal, dominant disorder with characteristic features that inc...
LEOPARD syndrome (LS) is an autosomal dominantly inherited or sporadic disorder of variable penetran...
The aim of this study was to characterize cardiovascular involvement in a large number of patients w...
Multiple lentigines syndrome is an autosomal dominant inherited condition with variable expressivity...
Background/PurposeLEOPARD syndrome (LS) is a rare, autosomal dominant disorder. The typical clinical...
LEOPARD syndrome (LS) is a rare, autosomal dominant disorder. The typical clinical presentation incl...
LEOPARD syndrome (LS) is a rare inherited autosomal dominant disease with high penetrance and marked...
LEOPARD syndrome (LS) is an autosomal dominant syndrome characterized by multiple lentigines and caf...
radiation dose cardiac CT A teenager with LEOPARD (‘cardiocutaneous’) syndrome,1 a rare autosomal do...
The LEOPARD syndrome is a rare, autosomal dominant multisystemic disorder characterized by lentigino...
Leopard Syndrome is a extremely rare disease, autosomal dominant, characterized from a series of sys...
LEOPARD syndrome, also known as Gorlin syndrome II, cardiocutaneous syndrome, lentiginosis profusa s...
is an autosomal dominant multiple congenital anom-aly syndrome, with high penetrance and markedly va...
Abstract LEOPARD syndrome (OMIM #151,100) caused by a germline PTPN11 mutation are characterized as ...
AbstractLEOPARD syndrome is a phenotypic expression of mutations in several genes: PTPN11, RAF1, and...
The L.E.O.P.A.R.D. syndrome is an autosomal, dominant disorder with characteristic features that inc...
LEOPARD syndrome (LS) is an autosomal dominantly inherited or sporadic disorder of variable penetran...
The aim of this study was to characterize cardiovascular involvement in a large number of patients w...
Multiple lentigines syndrome is an autosomal dominant inherited condition with variable expressivity...
Background/PurposeLEOPARD syndrome (LS) is a rare, autosomal dominant disorder. The typical clinical...
LEOPARD syndrome (LS) is a rare, autosomal dominant disorder. The typical clinical presentation incl...
LEOPARD syndrome (LS) is a rare inherited autosomal dominant disease with high penetrance and marked...
LEOPARD syndrome (LS) is an autosomal dominant syndrome characterized by multiple lentigines and caf...
radiation dose cardiac CT A teenager with LEOPARD (‘cardiocutaneous’) syndrome,1 a rare autosomal do...
The LEOPARD syndrome is a rare, autosomal dominant multisystemic disorder characterized by lentigino...
Leopard Syndrome is a extremely rare disease, autosomal dominant, characterized from a series of sys...
LEOPARD syndrome, also known as Gorlin syndrome II, cardiocutaneous syndrome, lentiginosis profusa s...