<?xml version="1.0" encoding="UTF-8"?>
<records>
<record>
<language>eng</language>
<publisher>Science and Education Publishing</publisher>
<journalTitle>American Journal of Medical Case Reports</journalTitle>
<eissn>2374-216X</eissn>
<publicationDate>2015-04-12</publicationDate>
<volume>3</volume>
<issue>4</issue>
<startPage>117</startPage>
<endPage>120</endPage>
<doi>10.12691/ajmcr-3-4-9</doi>
<publisherRecordId>AJMCR2015349</publisherRecordId>
<documentType>article</documentType>
<title language="eng">Gilbert's Syndrome Successfully Treated with the Paleolithic Ketogenic Diet</title>
<authors>
<author>
<name>Csaba Tóth</name>
<affiliationId>1</affiliationId>
</author>
<author>
<name>Zsófia Clemens</name>
<email>clemenszsofia@gmail.com</email>
<affiliationId>1</affiliationId>
<affiliationId>2</affiliationId>
</author>

</authors>
<affiliationsList>
<affiliationName affiliationId="1">Paleomedicina Hungary Ltd., Evolutionary Medicine Working Group, Budapest, H-1026 Hidász u. 3/A, Hungary</affiliationName>

</affiliationsList>
<abstract language="eng">Gilbert's syndrome (GS) is a common hyperbilirubinaemia syndrome caused by reduced conjugation of serum bilirubin by the liver. Although it is considered as a common and harmless condition not requiring treatment symptoms associated with GS may be unfavorable. Here we present a case of GS where high level of total and direct bilirubin, yellowish discoloration of the sclera as well as associated symptoms including migraine, fatigue and granulomatosus dermatitis were reversed following a shift toward the popular paleolithic and then toward the paleolithic ketogenic diet.</abstract>
<fullTextUrl format="pdf">http://pubs.sciepub.com/ajmcr/3/4/9/ajmcr-3-4-9.pdf</fullTextUrl>
<keywords language="eng"><keyword>Gilbert's syndrome</keyword>
<keyword>Paleolithic ketogenic diet</keyword>
<keyword>hyperbilirubinaemia</keyword>
<keyword>liver function</keyword>
</keywords>
</record>
</records>
