Add to ORKG<em>The data of clinical and instrumental examination of two infantile patients with obstructive hypertrophic cardiomyopathy in association with marked multisystem involvement as a picture of inherited malformation syndromes are given.</em><br /><strong><em>Key words: infants, hypertrophic cardiomyopathy, LEOPARD syndrome, Noonan syndrome.</em></strong><br /><span style="text-decoration: underline;"><em><em><em>(Voprosy sovremennoi pediatrii — Current Pediatrics. </em></em></em><em><em><em>2011; 10 (3): 166–169)</em></em></em></span
Aims: Children presenting with hypertrophic cardiomyopathy (HCM) in infancy are reported to have a p...
Abstract Noonan syndrome is a relatively common and heterogeneous genetic disorder, including congen...
suMMARY Experience has shown that clinical hypertrophic cardiomyopathy (HOCM, ASH) occurs in some pa...
Background: Hypertrophic cardiomyopathy, one of the most common inherited cardiomyopathies, is a het...
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...
Background: Hypertrophic cardiomyopathy is a rather common hereditary disease with an autozomal domi...
LEOPARD syndrome (multiple Lentigines, Electrocardiographic conduction abnormalities, Ocular hyperte...
Hypertrophic cardiomyopathy (HCM) is an inherited autosomal dominant disorder with variable penetran...
Hypertrophic cardiomyopathy is the most common form of cardiomyopathy, occurring in childhood, occur...
Multiple lentigines syndrome is an autosomal dominant inherited condition with variable expressivity...
Paediatric cardiomyopathies are a heterogenous group of rare disorders, characterised by mechanical ...
BACKGROUND: Nonsyndromic hypertrophic cardiomyopathy (HCM) is a primary cardiac disease transmitted ...
BACKGROUND: Nonsyndromic hypertrophic cardiomyopathy (HCM) is a primary cardiac disease transmitted ...
Hypertrophic cardiomyopathy (HCM) in neonates is a rare and heterogeneous disorder which is characte...
Aims: Children presenting with hypertrophic cardiomyopathy (HCM) in infancy are reported to have a p...
Abstract Noonan syndrome is a relatively common and heterogeneous genetic disorder, including congen...
suMMARY Experience has shown that clinical hypertrophic cardiomyopathy (HOCM, ASH) occurs in some pa...
Background: Hypertrophic cardiomyopathy, one of the most common inherited cardiomyopathies, is a het...
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...
Background: Hypertrophic cardiomyopathy is a rather common hereditary disease with an autozomal domi...
LEOPARD syndrome (multiple Lentigines, Electrocardiographic conduction abnormalities, Ocular hyperte...
Hypertrophic cardiomyopathy (HCM) is an inherited autosomal dominant disorder with variable penetran...
Hypertrophic cardiomyopathy is the most common form of cardiomyopathy, occurring in childhood, occur...
Multiple lentigines syndrome is an autosomal dominant inherited condition with variable expressivity...
Paediatric cardiomyopathies are a heterogenous group of rare disorders, characterised by mechanical ...
BACKGROUND: Nonsyndromic hypertrophic cardiomyopathy (HCM) is a primary cardiac disease transmitted ...
BACKGROUND: Nonsyndromic hypertrophic cardiomyopathy (HCM) is a primary cardiac disease transmitted ...
Hypertrophic cardiomyopathy (HCM) in neonates is a rare and heterogeneous disorder which is characte...
Aims: Children presenting with hypertrophic cardiomyopathy (HCM) in infancy are reported to have a p...
Abstract Noonan syndrome is a relatively common and heterogeneous genetic disorder, including congen...
suMMARY Experience has shown that clinical hypertrophic cardiomyopathy (HOCM, ASH) occurs in some pa...