Noonan's syndrome with extensive verrucae.
Identifieur interne : 005D13 ( PubMed/Corpus ); précédent : 005D12; suivant : 005D14Noonan's syndrome with extensive verrucae.
Auteurs : J. Bernier-Buzzanga ; W P SuSource :
- Cutis [ 0011-4162 ] ; 1990.
English descriptors
- KwdEn :
- MESH :
- complications : Lymphedema.
- congenital : Lymphedema.
- pathology : Noonan Syndrome, Warts.
- Adult, Humans, Male.
Abstract
We report the case of a patient with multiple findings characteristic of Noonan's syndrome, including a severe lymphedema present since early infancy, hypertelorism, low-set and prominent ears, broad facies, low posterior hairline, high arched palate, broad short neck, slightly short stature, and moderate dental malocclusion. In addition, extensive verrucae planae, verrucae vulgares, and condylomata acuminata occurred and were refractory to conventional therapy. To our knowledge, this is the first report of an association of Noonan's syndrome with extensive verrucae. We speculate that it is related to immunodeficiency as a consequence of loss of immunoglobulins and lymphocytes from intestinal lymphangiectasia. Cutaneous findings and other physical anomalies reported in patients with Noonan's syndrome are reviewed.
PubMed: 2225932
Links to Exploration step
pubmed:2225932Le document en format XML
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Bernier-Buzzanga</name><affiliation><nlm:affiliation>Department of Dermatology, Mayo Clinic, Rochester, Minnesota 55905.</nlm:affiliation></affiliation></author><author><name sortKey="Su, W P" sort="Su, W P" uniqKey="Su W" first="W P" last="Su">W P Su</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="1990">1990</date><idno type="RBID">pubmed:2225932</idno><idno type="pmid">2225932</idno><idno type="wicri:Area/PubMed/Corpus">005D13</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">005D13</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Noonan's syndrome with extensive verrucae.</title><author><name sortKey="Bernier Buzzanga, J" sort="Bernier Buzzanga, J" uniqKey="Bernier Buzzanga J" first="J" last="Bernier-Buzzanga">J. Bernier-Buzzanga</name><affiliation><nlm:affiliation>Department of Dermatology, Mayo Clinic, Rochester, Minnesota 55905.</nlm:affiliation></affiliation></author><author><name sortKey="Su, W P" sort="Su, W P" uniqKey="Su W" first="W P" last="Su">W P Su</name></author></analytic><series><title level="j">Cutis</title><idno type="ISSN">0011-4162</idno><imprint><date when="1990" type="published">1990</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term><term>Humans</term><term>Lymphedema (complications)</term><term>Lymphedema (congenital)</term><term>Male</term><term>Noonan Syndrome (pathology)</term><term>Warts (pathology)</term></keywords><keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="congenital" xml:lang="en"><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Noonan Syndrome</term><term>Warts</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adult</term><term>Humans</term><term>Male</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">We report the case of a patient with multiple findings characteristic of Noonan's syndrome, including a severe lymphedema present since early infancy, hypertelorism, low-set and prominent ears, broad facies, low posterior hairline, high arched palate, broad short neck, slightly short stature, and moderate dental malocclusion. In addition, extensive verrucae planae, verrucae vulgares, and condylomata acuminata occurred and were refractory to conventional therapy. To our knowledge, this is the first report of an association of Noonan's syndrome with extensive verrucae. We speculate that it is related to immunodeficiency as a consequence of loss of immunoglobulins and lymphocytes from intestinal lymphangiectasia. Cutaneous findings and other physical anomalies reported in patients with Noonan's syndrome are reviewed.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">2225932</PMID><DateCreated><Year>1990</Year><Month>12</Month><Day>12</Day></DateCreated><DateCompleted><Year>1990</Year><Month>12</Month><Day>12</Day></DateCompleted><DateRevised><Year>2013</Year><Month>09</Month><Day>12</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0011-4162</ISSN><JournalIssue CitedMedium="Print"><Volume>46</Volume><Issue>3</Issue><PubDate><Year>1990</Year><Month>Sep</Month></PubDate></JournalIssue><Title>Cutis</Title><ISOAbbreviation>Cutis</ISOAbbreviation></Journal><ArticleTitle>Noonan's syndrome with extensive verrucae.</ArticleTitle><Pagination><MedlinePgn>242-6</MedlinePgn></Pagination><Abstract><AbstractText>We report the case of a patient with multiple findings characteristic of Noonan's syndrome, including a severe lymphedema present since early infancy, hypertelorism, low-set and prominent ears, broad facies, low posterior hairline, high arched palate, broad short neck, slightly short stature, and moderate dental malocclusion. In addition, extensive verrucae planae, verrucae vulgares, and condylomata acuminata occurred and were refractory to conventional therapy. To our knowledge, this is the first report of an association of Noonan's syndrome with extensive verrucae. We speculate that it is related to immunodeficiency as a consequence of loss of immunoglobulins and lymphocytes from intestinal lymphangiectasia. Cutaneous findings and other physical anomalies reported in patients with Noonan's syndrome are reviewed.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Bernier-Buzzanga</LastName><ForeName>J</ForeName><Initials>J</Initials><AffiliationInfo><Affiliation>Department of Dermatology, Mayo Clinic, Rochester, Minnesota 55905.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Su</LastName><ForeName>W P</ForeName><Initials>WP</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Cutis</MedlineTA><NlmUniqueID>0006440</NlmUniqueID><ISSNLinking>0011-4162</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000328" MajorTopicYN="N">Adult</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008209" MajorTopicYN="N">Lymphedema</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName><QualifierName UI="Q000151" MajorTopicYN="N">congenital</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D009634" MajorTopicYN="N">Noonan Syndrome</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D014860" MajorTopicYN="N">Warts</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1990</Year><Month>9</Month><Day>1</Day></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>1990</Year><Month>9</Month><Day>1</Day><Hour>0</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>1990</Year><Month>9</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">2225932</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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