[Eye symptoms in connatal lymphedema].
Identifieur interne : 009C83 ( Ncbi/Checkpoint ); 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
Affiliations:
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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>
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<author><name sortKey="Mucke, J" sort="Mucke, J" uniqKey="Mucke J" first="J" last="Mücke">J. Mücke</name>
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<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>
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<series><title level="j">Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde</title>
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<imprint><date when="1985" type="published">1985</date>
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<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>
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<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>
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<name sortKey="Mucke, J" sort="Mucke, J" uniqKey="Mucke J" first="J" last="Mücke">J. Mücke</name>
</noCountry>
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