[Eye symptoms in connatal lymphedema].
Identifieur interne : 009C83 ( Ncbi/Merge ); précédent : 009C82; suivant : 009C84[Eye symptoms in connatal lymphedema].
Auteurs : H. Gornig ; J. MückeSource :
- Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde [ 0030-3755 ] ; 1985.
Descripteurs français
- KwdFr :
- MESH :
- génétique : Blépharoptose, Lymphoedème, Maladies de la conjonctive.
- malformations : Système lymphatique.
- Enfant, Enfant d'âge préscolaire, Humains, Lymphographie, Mâle.
English descriptors
- KwdEn :
- MESH :
- abnormalities : Lymphatic System.
- genetics : Blepharoptosis, Conjunctival Diseases, Lymphedema.
- Child, Child, Preschool, Humans, Lymphography, Male.
Abstract
Two brothers with symptoms of connate ophthalmic lymphatic oedema are reported. The combination--connate generalized lymphatic oedema with antimongoloid eyelid, 'cow-eye phenomenon', euryblepharon and conjunctival lymphatic oedema of two brothers with healthy parents--suggests the existence of a new entity of this syndrome with recessive heredity.
PubMed: 4080312
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 006846
- to stream PubMed, to step Curation: 006846
- to stream PubMed, to step Checkpoint: 006846
Links to Exploration step
pubmed:4080312Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">[Eye symptoms in connatal lymphedema].</title>
<author><name sortKey="Gornig, H" sort="Gornig, H" uniqKey="Gornig H" first="H" last="Gornig">H. Gornig</name>
</author>
<author><name sortKey="Mucke, J" sort="Mucke, J" uniqKey="Mucke J" first="J" last="Mücke">J. Mücke</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="1985">1985</date>
<idno type="RBID">pubmed:4080312</idno>
<idno type="pmid">4080312</idno>
<idno type="wicri:Area/PubMed/Corpus">006846</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">006846</idno>
<idno type="wicri:Area/PubMed/Curation">006846</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">006846</idno>
<idno type="wicri:Area/PubMed/Checkpoint">006846</idno>
<idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">006846</idno>
<idno type="wicri:Area/Ncbi/Merge">009C83</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en">[Eye symptoms in connatal lymphedema].</title>
<author><name sortKey="Gornig, H" sort="Gornig, H" uniqKey="Gornig H" first="H" last="Gornig">H. Gornig</name>
</author>
<author><name sortKey="Mucke, J" sort="Mucke, J" uniqKey="Mucke J" first="J" last="Mücke">J. Mücke</name>
</author>
</analytic>
<series><title level="j">Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde</title>
<idno type="ISSN">0030-3755</idno>
<imprint><date when="1985" type="published">1985</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Blepharoptosis (genetics)</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Conjunctival Diseases (genetics)</term>
<term>Humans</term>
<term>Lymphatic System (abnormalities)</term>
<term>Lymphedema (genetics)</term>
<term>Lymphography</term>
<term>Male</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Blépharoptose (génétique)</term>
<term>Enfant</term>
<term>Enfant d'âge préscolaire</term>
<term>Humains</term>
<term>Lymphoedème (génétique)</term>
<term>Lymphographie</term>
<term>Maladies de la conjonctive (génétique)</term>
<term>Mâle</term>
<term>Système lymphatique (malformations)</term>
</keywords>
<keywords scheme="MESH" qualifier="abnormalities" xml:lang="en"><term>Lymphatic System</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Blepharoptosis</term>
<term>Conjunctival Diseases</term>
<term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Blépharoptose</term>
<term>Lymphoedème</term>
<term>Maladies de la conjonctive</term>
</keywords>
<keywords scheme="MESH" qualifier="malformations" xml:lang="fr"><term>Système lymphatique</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Child</term>
<term>Child, Preschool</term>
<term>Humans</term>
<term>Lymphography</term>
<term>Male</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Enfant</term>
<term>Enfant d'âge préscolaire</term>
<term>Humains</term>
<term>Lymphographie</term>
<term>Mâle</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Two brothers with symptoms of connate ophthalmic lymphatic oedema are reported. The combination--connate generalized lymphatic oedema with antimongoloid eyelid, 'cow-eye phenomenon', euryblepharon and conjunctival lymphatic oedema of two brothers with healthy parents--suggests the existence of a new entity of this syndrome with recessive heredity.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">4080312</PMID>
<DateCreated><Year>1986</Year>
<Month>02</Month>
<Day>12</Day>
</DateCreated>
<DateCompleted><Year>1986</Year>
<Month>02</Month>
<Day>12</Day>
</DateCompleted>
<DateRevised><Year>2007</Year>
<Month>09</Month>
<Day>17</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">0030-3755</ISSN>
<JournalIssue CitedMedium="Print"><Volume>191</Volume>
<Issue>3</Issue>
<PubDate><Year>1985</Year>
</PubDate>
</JournalIssue>
<Title>Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde</Title>
<ISOAbbreviation>Ophthalmologica</ISOAbbreviation>
</Journal>
<ArticleTitle>[Eye symptoms in connatal lymphedema].</ArticleTitle>
<Pagination><MedlinePgn>133-8</MedlinePgn>
</Pagination>
<Abstract><AbstractText>Two brothers with symptoms of connate ophthalmic lymphatic oedema are reported. The combination--connate generalized lymphatic oedema with antimongoloid eyelid, 'cow-eye phenomenon', euryblepharon and conjunctival lymphatic oedema of two brothers with healthy parents--suggests the existence of a new entity of this syndrome with recessive heredity.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Gornig</LastName>
<ForeName>H</ForeName>
<Initials>H</Initials>
</Author>
<Author ValidYN="Y"><LastName>Mücke</LastName>
<ForeName>J</ForeName>
<Initials>J</Initials>
</Author>
</AuthorList>
<Language>ger</Language>
<PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType>
<PublicationType UI="D004740">English Abstract</PublicationType>
<PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<VernacularTitle>Augensymptome bei konnatalem Lymphödem.</VernacularTitle>
</Article>
<MedlineJournalInfo><Country>Switzerland</Country>
<MedlineTA>Ophthalmologica</MedlineTA>
<NlmUniqueID>0054655</NlmUniqueID>
<ISSNLinking>0030-3755</ISSNLinking>
</MedlineJournalInfo>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D001763" MajorTopicYN="N">Blepharoptosis</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002648" MajorTopicYN="N">Child</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002675" MajorTopicYN="N">Child, Preschool</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D003229" MajorTopicYN="N">Conjunctival Diseases</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008208" MajorTopicYN="N">Lymphatic System</DescriptorName>
<QualifierName UI="Q000002" MajorTopicYN="N">abnormalities</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008209" MajorTopicYN="N">Lymphedema</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008220" MajorTopicYN="N">Lymphography</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1985</Year>
<Month>1</Month>
<Day>1</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline"><Year>1985</Year>
<Month>1</Month>
<Day>1</Day>
<Hour>0</Hour>
<Minute>1</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez"><Year>1985</Year>
<Month>1</Month>
<Day>1</Day>
<Hour>0</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">4080312</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
<affiliations><list></list>
<tree><noCountry><name sortKey="Gornig, H" sort="Gornig, H" uniqKey="Gornig H" first="H" last="Gornig">H. Gornig</name>
<name sortKey="Mucke, J" sort="Mucke, J" uniqKey="Mucke J" first="J" last="Mücke">J. Mücke</name>
</noCountry>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/Ncbi/Merge
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 009C83 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Ncbi/Merge/biblio.hfd -nk 009C83 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Sante |area= LymphedemaV1 |flux= Ncbi |étape= Merge |type= RBID |clé= pubmed:4080312 |texte= [Eye symptoms in connatal lymphedema]. }}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Ncbi/Merge/RBID.i -Sk "pubmed:4080312" \ | HfdSelect -Kh $EXPLOR_AREA/Data/Ncbi/Merge/biblio.hfd \ | NlmPubMed2Wicri -a LymphedemaV1
This area was generated with Dilib version V0.6.31. |