J Korean Orthop Assoc. 1977 Jun;12(2):241-246. Korean.
Published online May 16, 2019.
Copyright © 1977 by The Korean Orthopaedic Association
Case Report

Hypokalemic Familial Periodic Paralysis: A Report of 4 members in a family

Kwang Jin Rhee, Seung Ho Yune and Han Kee Chae

    This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

    Abstract

    Hypokalemic familial periodic paralysis is one of the rare familial disease characterized by recurrent and transient attacks of weakness or paralysis of the somatic musculature. Also, this disease is usually inherited as an autosomal dominant trait in most cases. During an attack, the plasma potassium falls as a rasults of shift of potassium from the extracellular to the intracelluar compartment, but there is no loss of total potassium from the body. We have experienced hypokalemic familial periodic paralysis recently which affected 4 members in a family,and report this disorder.


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