Search results
Results from the WOW.Com Content Network
However, the genetics of Brugada syndrome are complex, and it is likely that the condition results from the interactions of many genes. Because of these complex interactions, some members of a family who carry a particular mutation may show evidence of Brugada syndrome while other carrying the same mutation may not, referred to as variable ...
Romano–Ward syndrome is a descriptive term for a group of subtypes of long QT syndrome, specifically subtypes LQT1-6 and LQT9-16. [8] Several subtypes of Romano–Ward syndrome have been described based on the underlying genetic variant. [5] These subtypes differ in clinical presentation and their response to treatment.
Bartter syndrome: various, by type Brugada syndrome: various, by type Catecholaminergic polymorphic ventricular tachycardia (CPVT) Ryanodine receptor: Congenital hyperinsulinism: Inward-rectifier potassium ion channel: Cystic fibrosis: Chloride channel Dravet syndrome: Voltage-gated sodium channel: Episodic ataxia: Voltage-gated potassium ...
A syndrome is a set of medical signs and symptoms that are correlated with each other. ... (Autosomal dominant inheritance: ... Brugada syndrome: Cantú syndrome ...
Long QT syndrome is estimated to affect 1 in 7,000 people. [6] Females are affected more often than males. [6] Most people with the condition develop symptoms before they are 40 years old. [6] It is a relatively common cause of sudden death along with Brugada syndrome and arrhythmogenic right ventricular dysplasia. [3]
In a 2008 study it was found that over half of SADS deaths could be attributed to inherited heart disease: unexplained premature sudden deaths in family, long QT syndrome, Brugada syndrome, arrhythmogenic right ventricular cardiomyopathy and others. [1]
758.0 Down syndrome; 758.1 Patau's syndrome; 758.2 Edward's syndrome; 758.3 Autosomal deletion syndromes 758.31 Cri du chat syndrome; 758.32 Velo-cardio-facial syndrome; 758.33 Other microdeletions. Miller–Dieker syndrome; Smith–Magenis syndrome; 758.4 Balanced autosomal translocation in normal individual; 758.5 Other conditions due to ...
A Systems Genetics Approach Identified GPD1L and its Molecular Mechanism for Obesity in Human Adipose Tissue This article on a gene on human chromosome 3 is a stub . You can help Wikipedia by expanding it .