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Article: Long term survival of a baby with homozygous alpha-thalassemia-1

TitleLong term survival of a baby with homozygous alpha-thalassemia-1
Authors
KeywordsHemoglobin Bart
Homozygous α-thalassemia-1
Issue Date1992
PublisherS Karger AG. The Journal's web site is located at http://www.karger.com/AHA
Citation
Acta Haematologica, 1992, v. 88 n. 4, p. 198-200 How to Cite?
AbstractTriplets born to a Chinese woman consisted of 2 healthy boys and a girl with hemoglobin Bart's hydrops syndrome. The girl with hemoglobin Bart's hydrops syndrome, confirmed by gene analysis to be homozygous for α-thalassemia-1, survives for 27 months at the time of reporting. The dilemma in sustaining her life and the availability of other therapeutic options are briefly discussed. This is the third case report of homozygous α-thalassemia-1 with long-term survival.
Persistent Identifierhttp://hdl.handle.net/10722/161958
ISSN
2023 Impact Factor: 1.7
2023 SCImago Journal Rankings: 0.686
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLam, TKen_US
dc.contributor.authorChan, Ven_US
dc.contributor.authorFok, TFen_US
dc.contributor.authorLi, CKen_US
dc.contributor.authorFeng, CSen_US
dc.date.accessioned2012-09-05T05:16:18Z-
dc.date.available2012-09-05T05:16:18Z-
dc.date.issued1992en_US
dc.identifier.citationActa Haematologica, 1992, v. 88 n. 4, p. 198-200en_US
dc.identifier.issn0001-5792en_US
dc.identifier.urihttp://hdl.handle.net/10722/161958-
dc.description.abstractTriplets born to a Chinese woman consisted of 2 healthy boys and a girl with hemoglobin Bart's hydrops syndrome. The girl with hemoglobin Bart's hydrops syndrome, confirmed by gene analysis to be homozygous for α-thalassemia-1, survives for 27 months at the time of reporting. The dilemma in sustaining her life and the availability of other therapeutic options are briefly discussed. This is the third case report of homozygous α-thalassemia-1 with long-term survival.en_US
dc.languageengen_US
dc.publisherS Karger AG. The Journal's web site is located at http://www.karger.com/AHAen_US
dc.relation.ispartofActa Haematologicaen_US
dc.subjectHemoglobin Bart-
dc.subjectHomozygous α-thalassemia-1-
dc.subject.meshChild, Preschoolen_US
dc.subject.meshChromosome Mappingen_US
dc.subject.meshDna - Blooden_US
dc.subject.meshEdema - Blood - Geneticsen_US
dc.subject.meshFemaleen_US
dc.subject.meshHemoglobins, Abnormal - Analysisen_US
dc.subject.meshHomozygoteen_US
dc.subject.meshHumansen_US
dc.subject.meshMaleen_US
dc.subject.meshRestriction Mappingen_US
dc.subject.meshSyndromeen_US
dc.subject.meshTripletsen_US
dc.subject.meshAlpha-Thalassemia - Blood - Geneticsen_US
dc.titleLong term survival of a baby with homozygous alpha-thalassemia-1en_US
dc.typeArticleen_US
dc.identifier.emailChan, V:vnychana@hkucc.hku.hken_US
dc.identifier.authorityChan, V=rp00320en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1159/000204686-
dc.identifier.pmid1292309-
dc.identifier.scopuseid_2-s2.0-0027052050en_US
dc.identifier.volume88en_US
dc.identifier.issue4en_US
dc.identifier.spage198en_US
dc.identifier.epage200en_US
dc.identifier.isiWOS:A1992KN36000007-
dc.publisher.placeSwitzerlanden_US
dc.identifier.scopusauthoridLam, TK=7202523143en_US
dc.identifier.scopusauthoridChan, V=7202654865en_US
dc.identifier.scopusauthoridFok, TF=7006455238en_US
dc.identifier.scopusauthoridLi, CK=15122650100en_US
dc.identifier.scopusauthoridFeng, CS=7402911517en_US
dc.identifier.issnl0001-5792-

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