LymphedemaV1, Ncbi, Merge, bibRecord, 004521

A photographic essay of prolidase deficiency.

Identifieur interne : 004521 ( Ncbi/Merge ); précédent : 004520; suivant : 004522

A photographic essay of prolidase deficiency.

Auteurs : Rebecca Dunn [Australie] ; George Varigos ; Ingrid Winship

Source :

Clinical dysmorphology [ 1473-5717 ] ; 2011.

RBID : pubmed:21760498

Descripteurs français

KwdFr :
- Adolescent, Adulte, Déficit en prolidase (diagnostic), Enfant, Humains, Jeune adulte, Maladies de la peau (anatomopathologie), Mâle, Phénotype.
MESH :
- anatomopathologie : Maladies de la peau.
- diagnostic : Déficit en prolidase.
- Adolescent, Adulte, Enfant, Humains, Jeune adulte, Mâle, Phénotype.

English descriptors

KwdEn :
- Adolescent, Adult, Child, Humans, Male, Phenotype, Prolidase Deficiency (diagnosis), Skin Diseases (pathology), Young Adult.
MESH :
- diagnosis : Prolidase Deficiency.
- pathology : Skin Diseases.
- Adolescent, Adult, Child, Humans, Male, Phenotype, Young Adult.

Abstract

Prolidase deficiency is a rare inherited connective tissue disorder characterised by intractable skin ulceration, lymphoedema, recurrent infections and mild intellectual impairment. We have documented the progress of an affected individual over the past 40 years, illustrated by high quality photographs to demonstrate the natural history of prolidase deficiency.

DOI: 10.1097/MCD.0b013e3283486cbd
PubMed: 21760498

Links toward previous steps (curation, corpus...)

to stream PubMed, to step Corpus: 002534
to stream PubMed, to step Curation: 002534
to stream PubMed, to step Checkpoint: 002534

Links to Exploration step

pubmed:21760498

Le document en format XML

<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">A photographic essay of prolidase deficiency.</title>
<author><name sortKey="Dunn, Rebecca" sort="Dunn, Rebecca" uniqKey="Dunn R" first="Rebecca" last="Dunn">Rebecca Dunn</name>
<affiliation wicri:level="1"><nlm:affiliation>Department of Dermatology, Royal Melbourne Hospital, Australia. rebecca_dunn@y7mail.com</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Department of Dermatology, Royal Melbourne Hospital</wicri:regionArea>
<wicri:noRegion>Royal Melbourne Hospital</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Varigos, George" sort="Varigos, George" uniqKey="Varigos G" first="George" last="Varigos">George Varigos</name>
</author>
<author><name sortKey="Winship, Ingrid" sort="Winship, Ingrid" uniqKey="Winship I" first="Ingrid" last="Winship">Ingrid Winship</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="2011">2011</date>
<idno type="RBID">pubmed:21760498</idno>
<idno type="pmid">21760498</idno>
<idno type="doi">10.1097/MCD.0b013e3283486cbd</idno>
<idno type="wicri:Area/PubMed/Corpus">002534</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">002534</idno>
<idno type="wicri:Area/PubMed/Curation">002534</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">002534</idno>
<idno type="wicri:Area/PubMed/Checkpoint">002534</idno>
<idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">002534</idno>
<idno type="wicri:Area/Ncbi/Merge">004521</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en">A photographic essay of prolidase deficiency.</title>
<author><name sortKey="Dunn, Rebecca" sort="Dunn, Rebecca" uniqKey="Dunn R" first="Rebecca" last="Dunn">Rebecca Dunn</name>
<affiliation wicri:level="1"><nlm:affiliation>Department of Dermatology, Royal Melbourne Hospital, Australia. rebecca_dunn@y7mail.com</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Department of Dermatology, Royal Melbourne Hospital</wicri:regionArea>
<wicri:noRegion>Royal Melbourne Hospital</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Varigos, George" sort="Varigos, George" uniqKey="Varigos G" first="George" last="Varigos">George Varigos</name>
</author>
<author><name sortKey="Winship, Ingrid" sort="Winship, Ingrid" uniqKey="Winship I" first="Ingrid" last="Winship">Ingrid Winship</name>
</author>
</analytic>
<series><title level="j">Clinical dysmorphology</title>
<idno type="eISSN">1473-5717</idno>
<imprint><date when="2011" type="published">2011</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adolescent</term>
<term>Adult</term>
<term>Child</term>
<term>Humans</term>
<term>Male</term>
<term>Phenotype</term>
<term>Prolidase Deficiency (diagnosis)</term>
<term>Skin Diseases (pathology)</term>
<term>Young Adult</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Adolescent</term>
<term>Adulte</term>
<term>Déficit en prolidase (diagnostic)</term>
<term>Enfant</term>
<term>Humains</term>
<term>Jeune adulte</term>
<term>Maladies de la peau (anatomopathologie)</term>
<term>Mâle</term>
<term>Phénotype</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Maladies de la peau</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Prolidase Deficiency</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Déficit en prolidase</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Skin Diseases</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adolescent</term>
<term>Adult</term>
<term>Child</term>
<term>Humans</term>
<term>Male</term>
<term>Phenotype</term>
<term>Young Adult</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Adolescent</term>
<term>Adulte</term>
<term>Enfant</term>
<term>Humains</term>
<term>Jeune adulte</term>
<term>Mâle</term>
<term>Phénotype</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Prolidase deficiency is a rare inherited connective tissue disorder characterised by intractable skin ulceration, lymphoedema, recurrent infections and mild intellectual impairment. We have documented the progress of an affected individual over the past 40 years, illustrated by high quality photographs to demonstrate the natural history of prolidase deficiency.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">21760498</PMID>
<DateCreated><Year>2011</Year>
<Month>09</Month>
<Day>08</Day>
</DateCreated>
<DateCompleted><Year>2012</Year>
<Month>01</Month>
<Day>17</Day>
</DateCompleted>
<DateRevised><Year>2011</Year>
<Month>09</Month>
<Day>08</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Electronic">1473-5717</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>20</Volume>
<Issue>4</Issue>
<PubDate><Year>2011</Year>
<Month>Oct</Month>
</PubDate>
</JournalIssue>
<Title>Clinical dysmorphology</Title>
<ISOAbbreviation>Clin. Dysmorphol.</ISOAbbreviation>
</Journal>
<ArticleTitle>A photographic essay of prolidase deficiency.</ArticleTitle>
<Pagination><MedlinePgn>194-9</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1097/MCD.0b013e3283486cbd</ELocationID>
<Abstract><AbstractText>Prolidase deficiency is a rare inherited connective tissue disorder characterised by intractable skin ulceration, lymphoedema, recurrent infections and mild intellectual impairment. We have documented the progress of an affected individual over the past 40 years, illustrated by high quality photographs to demonstrate the natural history of prolidase deficiency.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Dunn</LastName>
<ForeName>Rebecca</ForeName>
<Initials>R</Initials>
<AffiliationInfo><Affiliation>Department of Dermatology, Royal Melbourne Hospital, Australia. rebecca_dunn@y7mail.com</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Varigos</LastName>
<ForeName>George</ForeName>
<Initials>G</Initials>
</Author>
<Author ValidYN="Y"><LastName>Winship</LastName>
<ForeName>Ingrid</ForeName>
<Initials>I</Initials>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType>
<PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D016454">Review</PublicationType>
</PublicationTypeList>
</Article>
<MedlineJournalInfo><Country>England</Country>
<MedlineTA>Clin Dysmorphol</MedlineTA>
<NlmUniqueID>9207893</NlmUniqueID>
<ISSNLinking>0962-8827</ISSNLinking>
</MedlineJournalInfo>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D000293" MajorTopicYN="N">Adolescent</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D000328" MajorTopicYN="N">Adult</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002648" MajorTopicYN="N">Child</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D010641" MajorTopicYN="N">Phenotype</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D056732" MajorTopicYN="N">Prolidase Deficiency</DescriptorName>
<QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D012871" MajorTopicYN="N">Skin Diseases</DescriptorName>
<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D055815" MajorTopicYN="N">Young Adult</DescriptorName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2011</Year>
<Month>7</Month>
<Day>16</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed"><Year>2011</Year>
<Month>7</Month>
<Day>16</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline"><Year>2012</Year>
<Month>1</Month>
<Day>18</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">21760498</ArticleId>
<ArticleId IdType="doi">10.1097/MCD.0b013e3283486cbd</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
<affiliations><list><country><li>Australie</li>
</country>
</list>
<tree><noCountry><name sortKey="Varigos, George" sort="Varigos, George" uniqKey="Varigos G" first="George" last="Varigos">George Varigos</name>
<name sortKey="Winship, Ingrid" sort="Winship, Ingrid" uniqKey="Winship I" first="Ingrid" last="Winship">Ingrid Winship</name>
</noCountry>
<country name="Australie"><noRegion><name sortKey="Dunn, Rebecca" sort="Dunn, Rebecca" uniqKey="Dunn R" first="Rebecca" last="Dunn">Rebecca Dunn</name>
</noRegion>
</country>
</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 004521 | SxmlIndent | more

HfdSelect -h $EXPLOR_AREA/Data/Ncbi/Merge/biblio.hfd -nk 004521 | 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:21760498
   |texte=   A photographic essay of prolidase deficiency.
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/Ncbi/Merge/RBID.i   -Sk "pubmed:21760498" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Ncbi/Merge/biblio.hfd   \
       | NlmPubMed2Wicri -a LymphedemaV1

This area was generated with Dilib version V0.6.31.
Data generation: Sat Nov 4 17:40:35 2017. Site generation: Tue Feb 13 16:42:16 2024

	Serveur d'exploration sur le lymphœdème
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.

Serveur d'exploration sur le lymphœdème

A photographic essay of prolidase deficiency.

A photographic essay of prolidase deficiency.

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki