Aase-Smith syndrome type II

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dc.contributor.authorSoker, M
dc.contributor.authorAyyildiz, O
dc.contributor.authorIsikdogan, A
dc.date.accessioned2024-04-24T17:33:12Z
dc.date.available2024-04-24T17:33:12Z
dc.date.issued2004
dc.departmentDicle Üniversitesien_US
dc.description.abstractAase-Smith syndrome type II is rare in childhood and there are few reported cases. Here, we report an 8-month-old boy with congenital red cell aplasia and triphalangeal thumbs. In addition to thumb anomalies, he presented with growth failure, hypertelorism and novel osseous radiologic abnormalities, large fontanelles and micrognathia as extraordinary. Some clinical symptoms had complete clinical remission with deflazacort treatment.en_US
dc.identifier.endpage2006en_US
dc.identifier.issn0379-5284
dc.identifier.issue12en_US
dc.identifier.pmid15711686
dc.identifier.scopus2-s2.0-13844272218
dc.identifier.scopusqualityQ2
dc.identifier.startpage2004en_US
dc.identifier.urihttps://hdl.handle.net/11468/20527
dc.identifier.volume25en_US
dc.identifier.wosWOS:000226661000044
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoenen_US
dc.publisherSaudi Med Jen_US
dc.relation.ispartofSaudi Medical Journal
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject[No Keyword]en_US
dc.titleAase-Smith syndrome type IIen_US
dc.titleAase-Smith syndrome type II
dc.typeArticleen_US

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