Hereditary recurrent cholestasis with lymphoedema--two new families.
Identifieur interne : 00A107 ( Ncbi/Merge ); précédent : 00A106; suivant : 00A108Hereditary recurrent cholestasis with lymphoedema--two new families.
Auteurs : O. AagenaesSource :
- Acta paediatrica Scandinavica [ 0001-656X ] ; 1974.
Descripteurs français
- KwdFr :
- Adolescent, Biopsie, Cholestase (), Cholestase (anatomopathologie), Cholestase (génétique), Consanguinité, Enfant, Enfant d'âge préscolaire, Femelle, Foie (anatomopathologie), Humains, Ictère néonatal, Lymphoedème (), Lymphoedème (génétique), Mâle, Nourrisson, Nouveau-né, Pedigree, Récidive, Troubles de la croissance.
- MESH :
- anatomopathologie : Cholestase, Foie.
- génétique : Cholestase, Lymphoedème.
- Adolescent, Biopsie, Cholestase, Consanguinité, Enfant, Enfant d'âge préscolaire, Femelle, Humains, Ictère néonatal, Lymphoedème, Mâle, Nourrisson, Nouveau-né, Pedigree, Récidive, Troubles de la croissance.
English descriptors
- KwdEn :
- Adolescent, Biopsy, Child, Child, Preschool, Cholestasis (complications), Cholestasis (genetics), Cholestasis (pathology), Consanguinity, Female, Growth Disorders, Humans, Infant, Infant, Newborn, Jaundice, Neonatal, Liver (pathology), Lymphedema (complications), Lymphedema (genetics), Male, Pedigree, Recurrence.
- MESH :
- complications : Cholestasis, Lymphedema.
- genetics : Cholestasis, Lymphedema.
- pathology : Cholestasis, Liver.
- Adolescent, Biopsy, Child, Child, Preschool, Consanguinity, Female, Growth Disorders, Humans, Infant, Infant, Newborn, Jaundice, Neonatal, Male, Pedigree, Recurrence.
PubMed: 4857709
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 007431
- to stream PubMed, to step Curation: 007431
- to stream PubMed, to step Checkpoint: 007431
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pubmed:4857709Le document en format XML
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<series><title level="j">Acta paediatrica Scandinavica</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adolescent</term>
<term>Biopsy</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Cholestasis (complications)</term>
<term>Cholestasis (genetics)</term>
<term>Cholestasis (pathology)</term>
<term>Consanguinity</term>
<term>Female</term>
<term>Growth Disorders</term>
<term>Humans</term>
<term>Infant</term>
<term>Infant, Newborn</term>
<term>Jaundice, Neonatal</term>
<term>Liver (pathology)</term>
<term>Lymphedema (complications)</term>
<term>Lymphedema (genetics)</term>
<term>Male</term>
<term>Pedigree</term>
<term>Recurrence</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Adolescent</term>
<term>Biopsie</term>
<term>Cholestase ()</term>
<term>Cholestase (anatomopathologie)</term>
<term>Cholestase (génétique)</term>
<term>Consanguinité</term>
<term>Enfant</term>
<term>Enfant d'âge préscolaire</term>
<term>Femelle</term>
<term>Foie (anatomopathologie)</term>
<term>Humains</term>
<term>Ictère néonatal</term>
<term>Lymphoedème ()</term>
<term>Lymphoedème (génétique)</term>
<term>Mâle</term>
<term>Nourrisson</term>
<term>Nouveau-né</term>
<term>Pedigree</term>
<term>Récidive</term>
<term>Troubles de la croissance</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Cholestase</term>
<term>Foie</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Cholestasis</term>
<term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Cholestasis</term>
<term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Cholestase</term>
<term>Lymphoedème</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Cholestasis</term>
<term>Liver</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adolescent</term>
<term>Biopsy</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Consanguinity</term>
<term>Female</term>
<term>Growth Disorders</term>
<term>Humans</term>
<term>Infant</term>
<term>Infant, Newborn</term>
<term>Jaundice, Neonatal</term>
<term>Male</term>
<term>Pedigree</term>
<term>Recurrence</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Adolescent</term>
<term>Biopsie</term>
<term>Cholestase</term>
<term>Consanguinité</term>
<term>Enfant</term>
<term>Enfant d'âge préscolaire</term>
<term>Femelle</term>
<term>Humains</term>
<term>Ictère néonatal</term>
<term>Lymphoedème</term>
<term>Mâle</term>
<term>Nourrisson</term>
<term>Nouveau-né</term>
<term>Pedigree</term>
<term>Récidive</term>
<term>Troubles de la croissance</term>
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<DateCreated><Year>1974</Year>
<Month>08</Month>
<Day>23</Day>
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<DateCompleted><Year>1974</Year>
<Month>08</Month>
<Day>23</Day>
</DateCompleted>
<DateRevised><Year>2009</Year>
<Month>11</Month>
<Day>11</Day>
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<Article PubModel="Print"><Journal><ISSN IssnType="Print">0001-656X</ISSN>
<JournalIssue CitedMedium="Print"><Volume>63</Volume>
<Issue>3</Issue>
<PubDate><Year>1974</Year>
<Month>May</Month>
</PubDate>
</JournalIssue>
<Title>Acta paediatrica Scandinavica</Title>
<ISOAbbreviation>Acta Paediatr Scand</ISOAbbreviation>
</Journal>
<ArticleTitle>Hereditary recurrent cholestasis with lymphoedema--two new families.</ArticleTitle>
<Pagination><MedlinePgn>465-71</MedlinePgn>
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<Language>eng</Language>
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<MedlineJournalInfo><Country>Sweden</Country>
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<MeshHeadingList><MeshHeading><DescriptorName UI="D000293" MajorTopicYN="N">Adolescent</DescriptorName>
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<MeshHeading><DescriptorName UI="D001706" MajorTopicYN="N">Biopsy</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002648" MajorTopicYN="N">Child</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002675" MajorTopicYN="N">Child, Preschool</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002779" MajorTopicYN="N">Cholestasis</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D003241" MajorTopicYN="N">Consanguinity</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006130" MajorTopicYN="N">Growth Disorders</DescriptorName>
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<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
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<MeshHeading><DescriptorName UI="D007223" MajorTopicYN="N">Infant</DescriptorName>
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</MeshHeading>
<MeshHeading><DescriptorName UI="D007567" MajorTopicYN="N">Jaundice, Neonatal</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008099" MajorTopicYN="N">Liver</DescriptorName>
<QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008209" MajorTopicYN="N">Lymphedema</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D010375" MajorTopicYN="N">Pedigree</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D012008" MajorTopicYN="N">Recurrence</DescriptorName>
</MeshHeading>
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<PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1974</Year>
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<affiliations><list></list>
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