﻿<?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>2016-04-13</publicationDate>
    <volume>4</volume>
    <issue>3</issue>
    <startPage>97</startPage>
    <endPage>100</endPage>
    <doi>10.12691/ajmcr-4-3-7</doi>
    <publisherRecordId>AJMCR2016437</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Isolated Dislocation of Ocular Lens</title>
    <authors>
      <author>
        <name>Gabriela Acucella</name>
        <affiliationId>1</affiliationId>
      </author>
      <author>
        <name>Enrico Finale</name>
        <email>enrico.finale@gmail.com</email>
        <affiliationId>2</affiliationId>
      </author>
      <author>
        <name>Gaetano Auletta</name>
        <affiliationId>3</affiliationId>
      </author>
      <author>
        <name>Andrea Guala</name>
        <affiliationId>3</affiliationId>
      </author>
    </authors>
    <affiliationsList>
      <affiliationName affiliationId="1">Department of Pediatrics and Neonatology, Castelli Hospital, Verbania, Italy</affiliationName>
      <affiliationName affiliationId="2">Department of Obstetrics and Gynecology, Castelli Hospital, Verbania, Italy</affiliationName>
      <affiliationName affiliationId="3">University of Eastern Piedmont, Novara, Italy</affiliationName>
    </affiliationsList>
    <abstract language="eng">We describe a case of a child whit isolated dislocated of ocular lens, due to mutation in FBN1 gene. Differential syndromic diagnosis is made and we discuss to importance of clinical follow-up to exclude/confirm cardiologic complications due to Marfan syndrome.</abstract>
    <fullTextUrl format="pdf">http://pubs.sciepub.com/ajmcr/4/3/7/ajmcr-4-3-7.pdf</fullTextUrl>
    <keywords language="eng">
      <keyword>Ectopia lentis</keyword>
      <keyword>Fibrillin 1 gene</keyword>
      <keyword>Marfan syndrome</keyword>
    </keywords>
  </record>
</records>