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  <titleInfo>
    <title>Renal and retinal involvement in patients with bardet-biedl syndrome</title>
  </titleInfo>
  <titleInfo type="alternative">
    <title>دراسة تاثير الكلى وشبكية العين فى مرضى متلازمة باردت بيدل</title>
  </titleInfo>
  <name type="personal">
    <namePart>Rasha Helmy Mohamed Mohamed Elgendi</namePart>
    <role>
      <roleTerm authority="marcrelator" type="text">creator</roleTerm>
    </role>
  </name>
  <name type="personal">
    <namePart>Dina Mohamed Saied Elfayoumi</namePart>
    <role>
      <roleTerm type="text">Supervisor</roleTerm>
    </role>
  </name>
  <name type="personal">
    <namePart>Marwa Mohamed Ibrahim Nabhan</namePart>
    <role>
      <roleTerm type="text">Supervisor</roleTerm>
    </role>
  </name>
  <name type="personal">
    <namePart>Neveen Abdelmonem Soliman</namePart>
    <role>
      <roleTerm type="text">Supervisor</roleTerm>
    </role>
  </name>
  <typeOfResource>text</typeOfResource>
  <genre authority="marc">theses</genre>
  <originInfo>
    <place>
      <placeTerm type="code" authority="marccountry">ua</placeTerm>
    </place>
    <place>
      <placeTerm type="text">Cairo</placeTerm>
    </place>
    <publisher>Rasha Helmy Mohamed Mohamed Elgendi</publisher>
    <dateIssued>2013</dateIssued>
    <issuance>monographic</issuance>
  </originInfo>
  <language>
    <languageTerm authority="iso639-2b" type="code">eng</languageTerm>
  </language>
  <physicalDescription>
    <form authority="marcform">print</form>
    <extent>84 P. :  charts , facsimiles ;  25cm</extent>
  </physicalDescription>
  <abstract>Background : Bardet - biedl syndrome (BBS) is an autosomal recessive condition characterized by renal dysfunction rod- cone dystrophy postaxial polydactyly , obesity mental reardation and hypogonadism as a major criteria . Secondary features of BBS include speech delay strabismus , cataracts , brachydactyly syndactyly</abstract>
  <targetAudience authority="marctarget">specialized</targetAudience>
  <note type="statement of responsibility">Rasha Helmy Mohamed Mohamed Elgendi ; Supervised Neveen Abdelmonem Soliman , Marwa Mohamed Ibrahim Nabhan , Dina Mohamed Saied Elfayoumi</note>
  <note>Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Pediatrics</note>
  <note>Issued also as CD</note>
  <subject>
    <topic>Bardet- biedl  syndrome</topic>
  </subject>
  <subject>
    <topic>End stage kidney disease </topic>
  </subject>
  <subject>
    <topic>Retinitis pigmentosa </topic>
  </subject>
  <identifier type="uri">http://172.23.153.220/th.pdf</identifier>
  <location>
    <url>http://172.23.153.220/th.pdf</url>
  </location>
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    <recordContentSource authority="marcorg">EG-GiCUC</recordContentSource>
    <recordCreationDate encoding="marc">140324</recordCreationDate>
    <recordChangeDate encoding="iso8601">20250223030946.0</recordChangeDate>
    <languageOfCataloging>
      <languageTerm authority="iso639-2b" type="code">eng</languageTerm>
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