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Article: Subvalvular pulmonary stenosis, demyelination and myelodysplasia with monosomy 7

TitleSubvalvular pulmonary stenosis, demyelination and myelodysplasia with monosomy 7
Authors
KeywordsDemyelination
Monosomy 7
Myelodysplasia
Neurofibromatosis
Noonan syndrome
Pulmonary stenosis
Issue Date2002
PublisherInforma Healthcare. The Journal's web site is located at http://informahealthcare.com/loi/lal
Citation
Leukemia And Lymphoma, 2002, v. 43 n. 7, p. 1505-1507 How to Cite?
AbstractWe report a 23-year-old male with subvalvular pulmonary stenosis (PS) presenting with concurrent acute demyelinating neuropathy and myelodysplasia with monosomy 7. There was no stigmata of Noonan syndrome or neurofibromatosis, nor any family history of cardiac or hematologic disorders. There are 40 reported pediatric cases of Noonan syndrome with subvalvular PS that developed leukemia, over two-thirds with monosomy 7. There is also a genetic overlap between Noonan syndrome and neurofibromatosis, which is also closely associated with demyelination and leukemia. The importance of recognition of rare clinical syndromes that may predispose to leukemia is discussed.
Persistent Identifierhttp://hdl.handle.net/10722/76957
ISSN
2023 Impact Factor: 2.2
2023 SCImago Journal Rankings: 0.790
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorAu, WYen_HK
dc.contributor.authorMa, SKen_HK
dc.contributor.authorWan, TSen_HK
dc.contributor.authorJim, MHen_HK
dc.contributor.authorKwong, YLen_HK
dc.date.accessioned2010-09-06T07:26:44Z-
dc.date.available2010-09-06T07:26:44Z-
dc.date.issued2002en_HK
dc.identifier.citationLeukemia And Lymphoma, 2002, v. 43 n. 7, p. 1505-1507en_HK
dc.identifier.issn1042-8194en_HK
dc.identifier.urihttp://hdl.handle.net/10722/76957-
dc.description.abstractWe report a 23-year-old male with subvalvular pulmonary stenosis (PS) presenting with concurrent acute demyelinating neuropathy and myelodysplasia with monosomy 7. There was no stigmata of Noonan syndrome or neurofibromatosis, nor any family history of cardiac or hematologic disorders. There are 40 reported pediatric cases of Noonan syndrome with subvalvular PS that developed leukemia, over two-thirds with monosomy 7. There is also a genetic overlap between Noonan syndrome and neurofibromatosis, which is also closely associated with demyelination and leukemia. The importance of recognition of rare clinical syndromes that may predispose to leukemia is discussed.en_HK
dc.languageengen_HK
dc.publisherInforma Healthcare. The Journal's web site is located at http://informahealthcare.com/loi/lalen_HK
dc.relation.ispartofLeukemia and Lymphomaen_HK
dc.rightsLeukemia and Lymphoma. Copyright © Informa Healthcare.en_HK
dc.subjectDemyelinationen_HK
dc.subjectMonosomy 7en_HK
dc.subjectMyelodysplasiaen_HK
dc.subjectNeurofibromatosisen_HK
dc.subjectNoonan syndromeen_HK
dc.subjectPulmonary stenosisen_HK
dc.subject.meshAdult-
dc.subject.meshChromosomes, Human, Pair 7-
dc.subject.meshGuillain-Barre Syndrome - complications - diagnosis-
dc.subject.meshMyelodysplastic Syndromes - complications - diagnosis - genetics-
dc.subject.meshNoonan Syndrome - diagnosis - genetics-
dc.titleSubvalvular pulmonary stenosis, demyelination and myelodysplasia with monosomy 7en_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1042-8194&volume=43&issue=7&spage=1505&epage=1507&date=2002&atitle=Subvalvular+pulmonary+stenosis,+demyelination+and+myelodysplasia+with+monosomy+7en_HK
dc.identifier.emailKwong, YL:ylkwong@hku.hken_HK
dc.identifier.authorityKwong, YL=rp00358en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1080/1042819022386662en_HK
dc.identifier.pmid12389638-
dc.identifier.scopuseid_2-s2.0-85047685226en_HK
dc.identifier.hkuros77864en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0036299565&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume43en_HK
dc.identifier.issue7en_HK
dc.identifier.spage1505en_HK
dc.identifier.epage1507en_HK
dc.identifier.isiWOS:000176376900027-
dc.publisher.placeUnited Kingdomen_HK
dc.identifier.scopusauthoridAu, WY=7202383089en_HK
dc.identifier.scopusauthoridMa, SK=37020910400en_HK
dc.identifier.scopusauthoridWan, TS=25623981600en_HK
dc.identifier.scopusauthoridJim, MH=36784858000en_HK
dc.identifier.scopusauthoridKwong, YL=7102818954en_HK
dc.identifier.issnl1026-8022-

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