<?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>2015-07-24</publicationDate>
<volume>3</volume>
<issue>9</issue>
<startPage>269</startPage>
<endPage>271</endPage>
<doi>10.12691/ajmcr-3-9-1</doi>
<publisherRecordId>AJMCR2015391</publisherRecordId>
<documentType>article</documentType>
<title language="eng">Simultaneously Diagnosed Autoimmune Hepatitis Type II, Grave's Disease and Congenital Factor VII Deficiency</title>
<authors>
<author>
<name>Vanya Gerova</name>
<affiliationId>1</affiliationId>
</author>
<author>
<name>Ludmila Tankova</name>
<affiliationId>1</affiliationId>
</author>
<author>
<name>Ventsislav Nakov</name>
<affiliationId>1</affiliationId>
</author>
<author>
<name>Gergana Taneva</name>
<affiliationId>1</affiliationId>
</author>
<author>
<name>Radislav Nakov</name>
<email>radislav.nakov@gmail.com</email>
<affiliationId>1</affiliationId>
</author>

</authors>
<affiliationsList>
<affiliationName affiliationId="1">Clinical Center of Gastroenterology, „Queen Joanna” University Hospital, Sofia, Bulgaria</affiliationName>




</affiliationsList>
<abstract language="eng">Autoimmune hepatitis (AIH) is progressive, chronic immunologically mediated inflammatory liver disorder that occurs in children and adults of all ages, predominantly in women. AIH can be combined with other autoimmune and non-autoimmune conditions. We present a case of a 32 year-old female with three relatively uncommon diseases - two autoimmune diseases and one inherited, making their combination even more rare.</abstract>
<fullTextUrl format="pdf">http://pubs.sciepub.com/ajmcr/3/9/1/ajmcr-3-9-1.pdf</fullTextUrl>
<keywords language="eng"><keyword>autoimmune hepatitis type II</keyword>
<keyword>Grave's disease</keyword>
<keyword>congenital factor VII deficiency</keyword>
</keywords>
</record>
</records>
