Andersen-Tawil syndrome history and symptoms: Difference between revisions
Jump to navigation
Jump to search
Line 28: | Line 28: | ||
=== Common Symptoms === | === Common Symptoms === | ||
Common symptoms of Andersen-Tawil Syndrome include:<ref name="pmid12163457">{{cite journal| author=Tristani-Firouzi M, Jensen JL, Donaldson MR, Sansone V, Meola G, Hahn A | display-authors=etal| title=Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome). | journal=J Clin Invest | year= 2002 | volume= 110 | issue= 3 | pages= 381-8 | pmid=12163457 | doi=10.1172/JCI15183 | pmc=151085 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12163457 }}</ref> | Common symptoms of Andersen-Tawil Syndrome include:<ref name="pmid12163457">{{cite journal| author=Tristani-Firouzi M, Jensen JL, Donaldson MR, Sansone V, Meola G, Hahn A | display-authors=etal| title=Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome). | journal=J Clin Invest | year= 2002 | volume= 110 | issue= 3 | pages= 381-8 | pmid=12163457 | doi=10.1172/JCI15183 | pmc=151085 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12163457 }}</ref><ref name="pmid93072512">{{cite journal| author=Sansone V, Griggs RC, Meola G, Ptácek LJ, Barohn R, Iannaccone S | display-authors=etal| title=Andersen's syndrome: a distinct periodic paralysis. | journal=Ann Neurol | year= 1997 | volume= 42 | issue= 3 | pages= 305-12 | pmid=9307251 | doi=10.1002/ana.410420306 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9307251 }}</ref> | ||
* Periodic paralysis which are related to hypokalemia and are spontaneous in nature. | * Periodic paralysis which are related to hypokalemia and are spontaneous in nature. |
Revision as of 00:33, 5 February 2020
Andersen-Tawil syndrome Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Andersen-Tawil syndrome history and symptoms On the Web |
American Roentgen Ray Society Images of Andersen-Tawil syndrome history and symptoms |
Risk calculators and risk factors for Andersen-Tawil syndrome history and symptoms |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Charmaine Patel, M.D. [2]; Raviteja Guddeti, M.B.B.S. [3]
Symptoms
- Seizures - due to oxygen deprivation that occurs during arrhythmia.
- Fainting - fainting or syncope is the most common symptom LQTS.
- A prodrome may occur before losing consciousness, which may consist of lightheadedness, heart palpitations, blurred vision or weakness.
- Sudden death - a fatal arrhythmia that is not quickly intervened on, may cause sudden death.
History and Symptoms
- The majority of patients with [disease name] are asymptomatic.
OR
- The hallmark of [disease name] is [finding]. A positive history of [finding 1] and [finding 2] is suggestive of [disease name]. The most common symptoms of [disease name] include [symptom 1], [symptom 2], and [symptom 3].
- Symptoms of [disease name] include [symptom 1], [symptom 2], and [symptom 3].
History
Patients with Andersen-Tawil Syndrome may have a positive history of:
- Periodic paralysis
- Cardiac symptoms
- Ventricular arrhythmias
- [History finding 3]
Common Symptoms
Common symptoms of Andersen-Tawil Syndrome include:[1][2]
- Periodic paralysis which are related to hypokalemia and are spontaneous in nature.
- Ventricular arrhythmias.
- Extrasystoles:Premature ventricular contraction
- Arrhythmic syncope.
- Intermittent muscular weakness
- Skeletal developmental abnormalities
Less Common Symptoms
Less common symptoms of Andersen-Tawil Syndrome include:
- SCD(sudden cardiac death) is due to sudden hemodynamic collapse.
- SCA: Spinocerebellar ataxia.
- Generalized seizures, which are often misdiagnosed as primary seizure disorder.
- Learning difficulties.
References
- ↑ Tristani-Firouzi M, Jensen JL, Donaldson MR, Sansone V, Meola G, Hahn A; et al. (2002). "Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)". J Clin Invest. 110 (3): 381–8. doi:10.1172/JCI15183. PMC 151085. PMID 12163457.
- ↑ Sansone V, Griggs RC, Meola G, Ptácek LJ, Barohn R, Iannaccone S; et al. (1997). "Andersen's syndrome: a distinct periodic paralysis". Ann Neurol. 42 (3): 305–12. doi:10.1002/ana.410420306. PMID 9307251.