Multiple Endocrine Adenomatosis Type II (Sipple's Syndrome) in Twins
Identifieur interne : 002A74 ( Pmc/Checkpoint ); précédent : 002A73; suivant : 002A75Multiple Endocrine Adenomatosis Type II (Sipple's Syndrome) in Twins
Auteurs : Michael J. Reza ; Roy T. Young ; Andre J. Van Herle ; Vincent Dequattro ; Harold S. Cole ; Josiah BrownSource :
- Western Journal of Medicine [ 0093-0415 ] ; 1975.
Abstract
Medullary carcinoma of the thyroid, pheochromocytoma and multiple mucosal neuromas (MEA-II), a familial disorder of neuroectodermal tissue, is believed to be inherited in an autosomal dominant pattern. The occurrence of this syndrome in twins has not previously been reported. We have documented the presence of MEA-II in a pair of twins. The high incidence of bilaterality of pheochromocytoma is emphasized, as well as the usefulness of preoperative catecholamine fractionation, and vena cava catheterization sampling.
Url:
PubMed: 1199100
PubMed Central: 1130410
Affiliations:
Links toward previous steps (curation, corpus...)
Links to Exploration step
PMC:1130410Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Multiple Endocrine Adenomatosis Type II (Sipple's Syndrome) in Twins</title><author><name sortKey="Reza, Michael J" sort="Reza, Michael J" uniqKey="Reza M" first="Michael J." last="Reza">Michael J. Reza</name></author><author><name sortKey="Young, Roy T" sort="Young, Roy T" uniqKey="Young R" first="Roy T." last="Young">Roy T. Young</name></author><author><name sortKey="Van Herle, Andre J" sort="Van Herle, Andre J" uniqKey="Van Herle A" first="Andre J." last="Van Herle">Andre J. Van Herle</name></author><author><name sortKey="Dequattro, Vincent" sort="Dequattro, Vincent" uniqKey="Dequattro V" first="Vincent" last="Dequattro">Vincent Dequattro</name></author><author><name sortKey="Cole, Harold S" sort="Cole, Harold S" uniqKey="Cole H" first="Harold S." last="Cole">Harold S. Cole</name></author><author><name sortKey="Brown, Josiah" sort="Brown, Josiah" uniqKey="Brown J" first="Josiah" last="Brown">Josiah Brown</name></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">1199100</idno><idno type="pmc">1130410</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1130410</idno><idno type="RBID">PMC:1130410</idno><date when="1975">1975</date><idno type="wicri:Area/Pmc/Corpus">001835</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">001835</idno><idno type="wicri:Area/Pmc/Curation">001835</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Curation">001835</idno><idno type="wicri:Area/Pmc/Checkpoint">002A74</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Checkpoint">002A74</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Multiple Endocrine Adenomatosis Type II (Sipple's Syndrome) in Twins</title><author><name sortKey="Reza, Michael J" sort="Reza, Michael J" uniqKey="Reza M" first="Michael J." last="Reza">Michael J. Reza</name></author><author><name sortKey="Young, Roy T" sort="Young, Roy T" uniqKey="Young R" first="Roy T." last="Young">Roy T. Young</name></author><author><name sortKey="Van Herle, Andre J" sort="Van Herle, Andre J" uniqKey="Van Herle A" first="Andre J." last="Van Herle">Andre J. Van Herle</name></author><author><name sortKey="Dequattro, Vincent" sort="Dequattro, Vincent" uniqKey="Dequattro V" first="Vincent" last="Dequattro">Vincent Dequattro</name></author><author><name sortKey="Cole, Harold S" sort="Cole, Harold S" uniqKey="Cole H" first="Harold S." last="Cole">Harold S. Cole</name></author><author><name sortKey="Brown, Josiah" sort="Brown, Josiah" uniqKey="Brown J" first="Josiah" last="Brown">Josiah Brown</name></author></analytic><series><title level="j">Western Journal of Medicine</title><idno type="ISSN">0093-0415</idno><imprint><date when="1975">1975</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Medullary carcinoma of the thyroid, pheochromocytoma and multiple mucosal neuromas (MEA-II), a familial disorder of neuroectodermal tissue, is believed to be inherited in an autosomal dominant pattern. The occurrence of this syndrome in twins has not previously been reported. We have documented the presence of MEA-II in a pair of twins. The high incidence of bilaterality of pheochromocytoma is emphasized, as well as the usefulness of preoperative catecholamine fractionation, and vena cava catheterization sampling.</p><sec sec-type="scanned-figures"><title>Images</title><fig id="F1"><label>Figure 1.</label><graphic xlink:href="westjmed00292-0039-a" xlink:role="443"></graphic></fig><fig id="F2"><label>Figure 2.</label><graphic xlink:href="westjmed00292-0039-b" xlink:role="443"></graphic></fig><fig id="F3"><label>Figure 3.</label><graphic xlink:href="westjmed00292-0040-a" xlink:role="444"></graphic></fig><fig id="F4"><label>Figure 4</label><graphic xlink:href="westjmed00292-0041-a" xlink:role="445"></graphic></fig></sec></div></front></TEI><pmc article-type="research-article"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<front><journal-meta><journal-id journal-id-type="nlm-ta">West J Med</journal-id><journal-title>Western Journal of Medicine</journal-title><issn pub-type="ppub">0093-0415</issn></journal-meta><article-meta><article-id pub-id-type="pmid">1199100</article-id><article-id pub-id-type="pmc">1130410</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group></article-categories><title-group><article-title>Multiple Endocrine Adenomatosis Type II (Sipple's Syndrome) in Twins</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Reza</surname><given-names>Michael J.</given-names></name><degrees>MD</degrees> </contrib><contrib contrib-type="author"><name><surname>Young</surname><given-names>Roy T.</given-names></name><degrees>MD</degrees> </contrib><contrib contrib-type="author"><name><surname>Van Herle</surname><given-names>Andre J.</given-names></name><degrees>MD</degrees> </contrib><contrib contrib-type="author"><name><surname>DeQuattro</surname><given-names>Vincent</given-names></name><degrees>MD</degrees> </contrib><contrib contrib-type="author"><name><surname>Cole</surname><given-names>Harold S.</given-names></name><degrees>MD</degrees> </contrib><contrib contrib-type="author"><name><surname>Brown</surname><given-names>Josiah</given-names></name><degrees>MD</degrees> </contrib></contrib-group><aff id="af1">Division of Endocrinology, Department of Medicine, School of Medicine, University of California, Los Angeles</aff><aff id="af2">Department of Medicine, White Memorial Hospital, Loma Linda University, Los Angeles</aff><pub-date pub-type="ppub"><month>12</month><year>1975</year></pub-date><volume>123</volume><issue>6</issue><fpage>441</fpage><lpage>446</lpage><abstract><p>Medullary carcinoma of the thyroid, pheochromocytoma and multiple mucosal neuromas (MEA-II), a familial disorder of neuroectodermal tissue, is believed to be inherited in an autosomal dominant pattern. The occurrence of this syndrome in twins has not previously been reported. We have documented the presence of MEA-II in a pair of twins. The high incidence of bilaterality of pheochromocytoma is emphasized, as well as the usefulness of preoperative catecholamine fractionation, and vena cava catheterization sampling.</p><sec sec-type="scanned-figures"><title>Images</title><fig id="F1"><label>Figure 1.</label><graphic xlink:href="westjmed00292-0039-a" xlink:role="443"></graphic></fig><fig id="F2"><label>Figure 2.</label><graphic xlink:href="westjmed00292-0039-b" xlink:role="443"></graphic></fig><fig id="F3"><label>Figure 3.</label><graphic xlink:href="westjmed00292-0040-a" xlink:role="444"></graphic></fig><fig id="F4"><label>Figure 4</label><graphic xlink:href="westjmed00292-0041-a" xlink:role="445"></graphic></fig></sec></abstract></article-meta></front></pmc><affiliations><list></list><tree><noCountry><name sortKey="Brown, Josiah" sort="Brown, Josiah" uniqKey="Brown J" first="Josiah" last="Brown">Josiah Brown</name><name sortKey="Cole, Harold S" sort="Cole, Harold S" uniqKey="Cole H" first="Harold S." last="Cole">Harold S. Cole</name><name sortKey="Dequattro, Vincent" sort="Dequattro, Vincent" uniqKey="Dequattro V" first="Vincent" last="Dequattro">Vincent Dequattro</name><name sortKey="Reza, Michael J" sort="Reza, Michael J" uniqKey="Reza M" first="Michael J." last="Reza">Michael J. Reza</name><name sortKey="Van Herle, Andre J" sort="Van Herle, Andre J" uniqKey="Van Herle A" first="Andre J." last="Van Herle">Andre J. Van Herle</name><name sortKey="Young, Roy T" sort="Young, Roy T" uniqKey="Young R" first="Roy T." last="Young">Roy T. Young</name></noCountry></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/EdenteV2/Data/Pmc/Checkpoint
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 002A74 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Pmc/Checkpoint/biblio.hfd -nk 002A74 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Santé
|area= EdenteV2
|flux= Pmc
|étape= Checkpoint
|type= RBID
|clé= PMC:1130410
|texte= Multiple Endocrine Adenomatosis Type II (Sipple's Syndrome) in Twins
}}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Pmc/Checkpoint/RBID.i -Sk "pubmed:1199100" \
| HfdSelect -Kh $EXPLOR_AREA/Data/Pmc/Checkpoint/biblio.hfd \
| NlmPubMed2Wicri -a EdenteV2
| This area was generated with Dilib version V0.6.32. |  |