FAQ

Andersen Syndrome

Known as: ATS, Long QT Syndrome 7, Periodic Paralysis, Potassium-Sensitive Cardiodysrhythmic Type 
A form of inherited long QT syndrome (or LQT7) that is characterized by a triad of potassium-sensitive periodic paralysis, VENTRICULAR ECTOPIC BEATS… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1953-2018
010203019532017

Related topics

Related topics

25 relations
Anterior crossbiteAutosomal dominant inheritanceBrachydactylyByzanthine arch palate
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Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
Andersen Syndrome
radiotherapeutic
Autosomal dominant inheritance
Syncope
prevention & control
Scoliosis, unspecified

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2009
2009
Clinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/ COL4A4 genes associated with familial haematuria and…
BACKGROUND Heterozygous mutations in the COL4A3/ COL4A4 genes are currently thought to be responsible for familial benign… (More)
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2008
2008
Arterial tortuosity syndrome: clinical and molecular findings in 12 newly identified families.
Arterial tortuosity syndrome (ATS) is a rare autosomal recessive connective tissue disease, characterized by widespread arterial… (More)
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2007
2007
Genotype-phenotype correlations of KCNJ2 mutations in Japanese patients with Andersen-Tawil syndrome.
Andersen-Tawil syndrome (ATS) is a rare inherited disorder characterized by periodic paralysis, mild dysmorphic features, and QT… (More)
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2006
2006
Cellular basis for electrocardiographic and arrhythmic manifestations of Andersen-Tawil syndrome (LQT7).
BACKGROUND Andersen-Tawil syndrome, a skeletal muscle syndrome associated with periodic paralysis and long QT intervals on the… (More)
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Highly Cited
2005
Highly Cited
2005
Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype.
BACKGROUND The ECG features of Andersen-Tawil syndrome (ATS) patients with KCNJ2 mutations (ATS1) have not been systematically… (More)
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2005
2005
Andersen-Tawil syndrome: new potassium channel mutations and possible phenotypic variation.
OBJECTIVE To evaluate clinical, genetic, and electrophysiologic features of patients with Andersen-Tawil syndrome (ATS) in the… (More)
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2005
2005
Precocious intima-media thickening in patients with primary Sjögren's syndrome.
OBJECTIVE Systemic lupus erythematosus and rheumatoid arthritis represent independent risk factors for atherosclerosis (ATS… (More)
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Highly Cited
2003
Highly Cited
2003
PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome.
BACKGROUND Mutations in KCNJ2, the gene encoding the inward-rectifying K+ channel Kir2.1, cause the cardiac, skeletal muscle, and… (More)
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Highly Cited
2002
Highly Cited
2002
Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome).
Andersen syndrome (AS) is a rare, inherited disorder characterized by periodic paralysis, long QT (LQT) with ventricular… (More)
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Highly Cited
1994
Highly Cited
1994
Relations between performance and subjective ratings of sleepiness during a night awake.
The present study validated the nine-point Karolinska Sleepiness Scale (KSS) and the new Accumulated Time with Sleepiness (ATS… (More)
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