Familial yellow nail syndrome.
Identifieur interne : 007977 ( Main/Exploration ); précédent : 007976; suivant : 007978Familial yellow nail syndrome.
Auteurs : Ebrahim Razi [Iran]Source :
- Dermatology online journal [ 1087-2108 ] ; 2006.
Descripteurs français
- KwdFr :
- MESH :
- génétique : Hypoprotéinémie, Lymphoedème, Onychopathies, Troubles de la pigmentation, Épanchement pleural.
- Femelle, Humains, Sujet âgé, Syndrome.
English descriptors
- KwdEn :
- MESH :
- genetics : Hypoproteinemia, Lymphedema, Nail Diseases, Pigmentation Disorders, Pleural Effusion.
- Aged, Female, Humans, Syndrome.
Abstract
A 70-year-old woman with yellow nail syndrome and right-sided pleural effusion, lower extremity edema, and hypoalbuminemia was followed for 18 months. She reported an 8-year history of asthma. She had four children (3 boys and 1 girl). Dystrophy, changes in color and shape of nails both hands and foot, along with lower extremity edema was observed in the daughter and two of her sons. One son had asthma. The patient reported that her grandmother had similar nail abnormality and lower extremity edema. Other family members and patient's grandchildren were healthy. This report demonstrates a case of familial yellow-nail syndrome.
PubMed: 16638408
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 003A15
- to stream PubMed, to step Curation: 003A15
- to stream PubMed, to step Checkpoint: 003A15
- to stream Ncbi, to step Merge: 002206
- to stream Ncbi, to step Curation: 002206
- to stream Ncbi, to step Checkpoint: 002206
- to stream Main, to step Merge: 007B63
- to stream Main, to step Curation: 007977
Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Familial yellow nail syndrome.</title>
<author><name sortKey="Razi, Ebrahim" sort="Razi, Ebrahim" uniqKey="Razi E" first="Ebrahim" last="Razi">Ebrahim Razi</name>
<affiliation wicri:level="1"><nlm:affiliation>Section of Internal Medicine, Kashan University of Medical Sciences, Kashan, Iran. ebrahimrazi@yahoo.com</nlm:affiliation>
<country xml:lang="fr">Iran</country>
<wicri:regionArea>Section of Internal Medicine, Kashan University of Medical Sciences, Kashan</wicri:regionArea>
<wicri:noRegion>Kashan</wicri:noRegion>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="2006">2006</date>
<idno type="RBID">pubmed:16638408</idno>
<idno type="pmid">16638408</idno>
<idno type="wicri:Area/PubMed/Corpus">003A15</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">003A15</idno>
<idno type="wicri:Area/PubMed/Curation">003A15</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">003A15</idno>
<idno type="wicri:Area/PubMed/Checkpoint">003A15</idno>
<idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">003A15</idno>
<idno type="wicri:Area/Ncbi/Merge">002206</idno>
<idno type="wicri:Area/Ncbi/Curation">002206</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">002206</idno>
<idno type="wicri:Area/Main/Merge">007B63</idno>
<idno type="wicri:Area/Main/Curation">007977</idno>
<idno type="wicri:Area/Main/Exploration">007977</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en">Familial yellow nail syndrome.</title>
<author><name sortKey="Razi, Ebrahim" sort="Razi, Ebrahim" uniqKey="Razi E" first="Ebrahim" last="Razi">Ebrahim Razi</name>
<affiliation wicri:level="1"><nlm:affiliation>Section of Internal Medicine, Kashan University of Medical Sciences, Kashan, Iran. ebrahimrazi@yahoo.com</nlm:affiliation>
<country xml:lang="fr">Iran</country>
<wicri:regionArea>Section of Internal Medicine, Kashan University of Medical Sciences, Kashan</wicri:regionArea>
<wicri:noRegion>Kashan</wicri:noRegion>
</affiliation>
</author>
</analytic>
<series><title level="j">Dermatology online journal</title>
<idno type="eISSN">1087-2108</idno>
<imprint><date when="2006" type="published">2006</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term>
<term>Female</term>
<term>Humans</term>
<term>Hypoproteinemia (genetics)</term>
<term>Lymphedema (genetics)</term>
<term>Nail Diseases (genetics)</term>
<term>Pigmentation Disorders (genetics)</term>
<term>Pleural Effusion (genetics)</term>
<term>Syndrome</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Femelle</term>
<term>Humains</term>
<term>Hypoprotéinémie (génétique)</term>
<term>Lymphoedème (génétique)</term>
<term>Onychopathies (génétique)</term>
<term>Sujet âgé</term>
<term>Syndrome</term>
<term>Troubles de la pigmentation (génétique)</term>
<term>Épanchement pleural (génétique)</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Hypoproteinemia</term>
<term>Lymphedema</term>
<term>Nail Diseases</term>
<term>Pigmentation Disorders</term>
<term>Pleural Effusion</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Hypoprotéinémie</term>
<term>Lymphoedème</term>
<term>Onychopathies</term>
<term>Troubles de la pigmentation</term>
<term>Épanchement pleural</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Aged</term>
<term>Female</term>
<term>Humans</term>
<term>Syndrome</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Femelle</term>
<term>Humains</term>
<term>Sujet âgé</term>
<term>Syndrome</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">A 70-year-old woman with yellow nail syndrome and right-sided pleural effusion, lower extremity edema, and hypoalbuminemia was followed for 18 months. She reported an 8-year history of asthma. She had four children (3 boys and 1 girl). Dystrophy, changes in color and shape of nails both hands and foot, along with lower extremity edema was observed in the daughter and two of her sons. One son had asthma. The patient reported that her grandmother had similar nail abnormality and lower extremity edema. Other family members and patient's grandchildren were healthy. This report demonstrates a case of familial yellow-nail syndrome.</div>
</front>
</TEI>
<affiliations><list><country><li>Iran</li>
</country>
</list>
<tree><country name="Iran"><noRegion><name sortKey="Razi, Ebrahim" sort="Razi, Ebrahim" uniqKey="Razi E" first="Ebrahim" last="Razi">Ebrahim Razi</name>
</noRegion>
</country>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 007977 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 007977 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Sante |area= LymphedemaV1 |flux= Main |étape= Exploration |type= RBID |clé= pubmed:16638408 |texte= Familial yellow nail syndrome. }}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i -Sk "pubmed:16638408" \ | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd \ | NlmPubMed2Wicri -a LymphedemaV1
This area was generated with Dilib version V0.6.31. |