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dc.contributor.authorE. Ferda Perçin
dc.contributor.authorİlhan Sezgin
dc.contributor.authorSıtkı Perçin
dc.contributor.authorÖztürk Özdemir
dc.date.accessioned23.07.201910:49:13
dc.date.accessioned2019-07-23T16:19:28Z
dc.date.available23.07.201910:49:13
dc.date.available2019-07-23T16:19:28Z
dc.date.issued1997
dc.identifier.issn1300-199X
dc.identifier.urihttp://www.trdizin.gov.tr/publication/paper/detail/TkRJeU1qUTA=
dc.identifier.urihttps://hdl.handle.net/20.500.12418/859
dc.description.abstractAnne-babası akraba olmayan dört aylık erkek çocuğun mikroti, retromikrognati, hipoglossi gibi bulgularına ilaveten' sağ elinde ikinci, üçüncü, dördüncü parmak ve metakarplar, sağ ayağında da tüm parmak ve metatarslar yoktu. Bu bulgular nedeniyle oromandibuler-limb hipogehezis tanısı konuldu. Prenatal öyküden ilk trimesterde ilaç kullanımı olduğu öğrenildi ve olgu nadir görülmesi nedeniyle sunuldu.en_US
dc.description.abstractA four- month-old boy whose parents have no consanguineous marriage was diagnosed as having or-omandibular-limb hypogenesis. Clinical examination of the patient showed microtia, retromicrognathia, hypoglossia, absence of the second, third, fourth fingers at the right hand and associated metacarpals as well as absence of all toes and metatarsals at right foot. Since the prenatal history of the patient has shown that the mother had used medications during the first trimester of her pregnancy, the case was considered to be rare and reported.en_US
dc.language.isoturen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectGenel ve Dahili Tıpen_US
dc.titleOromandibular-limb hipogenezis spektrumlu bir olguen_US
dc.title.alternativeA case with oromandibular-limb hypogenesis spectrumen_US
dc.typeotheren_US
dc.relation.journalErciyes Tıp Dergisien_US
dc.contributor.departmentSivas Cumhuriyet Üniversitesien_US
dc.identifier.volume19en_US
dc.identifier.issue4en_US
dc.identifier.endpage232en_US
dc.identifier.startpage230en_US
dc.relation.publicationcategoryDiğeren_US]


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