| Andersen Tawil syndrome - periodic paralysis with dysmorphism. | |
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MedLine Citation:
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PMID: 21317470 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Andersen Tawil syndrome is a rare type of channelopathy characterized by the presence of periodic paralysis, cardiac arrhythmia (prolonged QT interval or ventricular arrhythmia) and distinct dysmorphic abnormalities. It is a type of potassium channelopathy that occurs sporadically or by autosomal dominant inheritance. We report a 14 year old boy with Andersen-Tawil syndrome. |
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Authors:
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Mahesh Kamate; Vivek Chetal |
Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Indian pediatrics Volume: 48 ISSN: 0974-7559 ISO Abbreviation: Indian Pediatr Publication Date: 2011 Jan |
Date Detail:
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Created Date: 2011-02-14 Completed Date: 2011-06-30 Revised Date: 2011-11-21 |
Medline Journal Info:
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Nlm Unique ID: 2985062R Medline TA: Indian Pediatr Country: India |
Other Details:
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Languages: eng Pagination: 64-5 Citation Subset: IM |
Affiliation:
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Department of Pediatrics, KLE University J N Medical College, Belgaum, Karnataka, India. drmaheshkamate@gmail.com |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Adolescent Andersen Syndrome / pathology, physiopathology Fingers / pathology Humans Male Paralysis |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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