Add to ORKGThree members of a family with features of the 'leopard' syndrome are described. The important findings were generalized lentigo, deafness, and cardiac and electrocardiographic abnormalities. Progressive obstructive cardiomyopathy and arrhythmias are features of the condition which may be present, and are potentially life-threatening.S. Afr. Med. J., 47, 1 (1973)
LEOPARD syndrome (LS) is an autosomal dominant syndrome characterized by multiple lentigines and caf...
AbstractLEOPARD syndrome, one of many cardiocutaneous syndromes, is an acronym for some of the obvio...
LEOPARD syndrome is a complex dysmorphogenetic disorder of variable penetrance and expressivity. Mut...
LEOPARD syndrome (LS) is an autosomal dominantly inherited or sporadic disorder of variable penetran...
Multiple lentigines syndrome is an autosomal dominant inherited condition with variable expressivity...
The LEOPARD syndrome is a rare, autosomal dominant multisystemic disorder characterized by lentigino...
Background: LEOPARD syndrome is a complex dysmorphogenetic disorder of inconstant penetrance and var...
ABSTRACT Hypertrophic cardiomyopathy is known as Leopard syndrome, which is a mnemonic rule for mult...
Abstract LEOPARD syndrome (LS, OMIM 151100) is a rare multiple congenital anomalies condition, mainl...
The aim of this study was to characterize cardiovascular involvement in a large number of patients w...
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...
LEOPARD syndrome (LS) is a rare inherited autosomal dominant disease with high penetrance and marked...
LEOPARD syndrome (multiple Lentigines, Electrocardiographic conduction abnormalities, Ocular hyperte...
LEOPARD syndrome (LS) is an autosomal dominant syndrome characterized by multiple lentigines and caf...
AbstractLEOPARD syndrome, one of many cardiocutaneous syndromes, is an acronym for some of the obvio...
LEOPARD syndrome is a complex dysmorphogenetic disorder of variable penetrance and expressivity. Mut...
LEOPARD syndrome (LS) is an autosomal dominantly inherited or sporadic disorder of variable penetran...
Multiple lentigines syndrome is an autosomal dominant inherited condition with variable expressivity...
The LEOPARD syndrome is a rare, autosomal dominant multisystemic disorder characterized by lentigino...
Background: LEOPARD syndrome is a complex dysmorphogenetic disorder of inconstant penetrance and var...
ABSTRACT Hypertrophic cardiomyopathy is known as Leopard syndrome, which is a mnemonic rule for mult...
Abstract LEOPARD syndrome (LS, OMIM 151100) is a rare multiple congenital anomalies condition, mainl...
The aim of this study was to characterize cardiovascular involvement in a large number of patients w...
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...
LEOPARD syndrome (LS) is a rare inherited autosomal dominant disease with high penetrance and marked...
LEOPARD syndrome (multiple Lentigines, Electrocardiographic conduction abnormalities, Ocular hyperte...
LEOPARD syndrome (LS) is an autosomal dominant syndrome characterized by multiple lentigines and caf...
AbstractLEOPARD syndrome, one of many cardiocutaneous syndromes, is an acronym for some of the obvio...
LEOPARD syndrome is a complex dysmorphogenetic disorder of variable penetrance and expressivity. Mut...