Abstract LEOPARD syndrome (LS, OMIM 151100) is a rare multiple congenital anomalies condition, mainly characterized by skin, facial and cardiac anomalies. LEOPARD is an acronym for the major features of this disorder, including multiple Lentigines, ECG conduction abnormalities, Ocular hypertelorism, Pulmonic stenosis, Abnormal genitalia, Retardation of growth, and sensorineural Deafness. About 200 patients have been reported worldwide but the real incidence of LS has not been assessed. Facial dysmorphism includes ocular hypertelorism, palpebral ptosis and low-set ears. Stature is usually below the 25th centile. Cardiac defects, in particular hypertrophic cardiomyopathy mostly involving the left ventricle, and ECG anomalies are common. The l...
LEOPARD multiple congenital anomaly syndrome inherited in an autosomal dominant manner. LEOPARD is a...
LEOPARD syndrome is a complex disorder characterized by multiple dysmorphogenetic features. Both syn...
LEOPARD syndrome (LS) is a congenital developmental disorder and is an acronym for multiple lentigin...
LEOPARD syndrome (LS) is an autosomal dominant syndrome characterized by multiple lentigines and caf...
Abstract LEOPARD syndrome (OMIM #151,100) caused by a germline PTPN11 mutation are characterized as ...
The L.E.O.P.A.R.D. syndrome is an autosomal, dominant disorder with characteristic features that inc...
AbstractLEOPARD syndrome is a phenotypic expression of mutations in several genes: PTPN11, RAF1, and...
LEOPARD syndrome (LS) is an autosomal dominantly inherited or sporadic disorder of variable penetran...
LEOPARD syndrome is a complex dysmorphogenetic disorder of variable penetrance and expressivity. Mut...
Multiple lentigines syndrome is an autosomal dominant inherited condition with variable expressivity...
ABSTRACT Hypertrophic cardiomyopathy is known as Leopard syndrome, which is a mnemonic rule for mult...
is an autosomal dominant multiple congenital anom-aly syndrome, with high penetrance and markedly va...
LEOPARD syndrome (LS) is a rare, autosomal dominant disorder. The typical clinical presentation incl...
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...
LEOPARD multiple congenital anomaly syndrome inherited in an autosomal dominant manner. LEOPARD is a...
LEOPARD syndrome is a complex disorder characterized by multiple dysmorphogenetic features. Both syn...
LEOPARD syndrome (LS) is a congenital developmental disorder and is an acronym for multiple lentigin...
LEOPARD syndrome (LS) is an autosomal dominant syndrome characterized by multiple lentigines and caf...
Abstract LEOPARD syndrome (OMIM #151,100) caused by a germline PTPN11 mutation are characterized as ...
The L.E.O.P.A.R.D. syndrome is an autosomal, dominant disorder with characteristic features that inc...
AbstractLEOPARD syndrome is a phenotypic expression of mutations in several genes: PTPN11, RAF1, and...
LEOPARD syndrome (LS) is an autosomal dominantly inherited or sporadic disorder of variable penetran...
LEOPARD syndrome is a complex dysmorphogenetic disorder of variable penetrance and expressivity. Mut...
Multiple lentigines syndrome is an autosomal dominant inherited condition with variable expressivity...
ABSTRACT Hypertrophic cardiomyopathy is known as Leopard syndrome, which is a mnemonic rule for mult...
is an autosomal dominant multiple congenital anom-aly syndrome, with high penetrance and markedly va...
LEOPARD syndrome (LS) is a rare, autosomal dominant disorder. The typical clinical presentation incl...
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...
LEOPARD multiple congenital anomaly syndrome inherited in an autosomal dominant manner. LEOPARD is a...
LEOPARD syndrome is a complex disorder characterized by multiple dysmorphogenetic features. Both syn...
LEOPARD syndrome (LS) is a congenital developmental disorder and is an acronym for multiple lentigin...