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dc.contributor.authorAslan, Mustafa Torehan
dc.contributor.authorCoban, Asuman
dc.contributor.authorInce, Elmas
dc.date.accessioned2021-12-10T11:00:54Z
dc.date.available2021-12-10T11:00:54Z
dc.date.issued2021
dc.identifier.citationAslan M. T. , Ince E., Coban A., "EARLY-ONSET CENTRAL DIABETES INSIPIDUS IN A NEWBORN WITH HOLOPROSENCEPHALY", JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI, cilt.84, sa.4, ss.599-602, 2021
dc.identifier.othervv_1032021
dc.identifier.otherav_62247e4e-b481-4020-886a-8f2b1b62a510
dc.identifier.urihttp://hdl.handle.net/20.500.12627/171033
dc.identifier.urihttps://doi.org/10.26650/iuitfd.2021.807168
dc.description.abstractHoloprosencephaly is a complex brain malformation caused by the inability of the prosencephalon to divide to form the cerebral hemispheres. Central diabetes insipidus (CDI), as a result of a defect in vasopressin release, may be seen due to the abnormal hypothalamic infundibular region. CDI developing secondary to holoprosencephaly in the early neonatal period has rarely been reported in the literature. A case of early-onset CDI with holoprosencephaly and 13q deletion is presented.
dc.language.isoeng
dc.subjectFundamentals and Skills
dc.subjectGeneral Health Professions
dc.subjectPathophysiology
dc.subjectInternal Medicine
dc.subjectAssessment and Diagnosis
dc.subjectMedicine (miscellaneous)
dc.subjectGeneral Medicine
dc.subjectHealth Sciences
dc.subjectTemel Tıp Bilimleri
dc.subjectFamily Practice
dc.subjectSağlık Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectKlinik Tıp
dc.subjectTIP, GENEL & İÇECEK
dc.titleEARLY-ONSET CENTRAL DIABETES INSIPIDUS IN A NEWBORN WITH HOLOPROSENCEPHALY
dc.typeMakale
dc.relation.journalJOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI
dc.contributor.departmentİstanbul Üniversitesi , İstanbul Tıp Fakültesi , Neonatoloji Bilim Dalı
dc.identifier.volume84
dc.identifier.issue4
dc.identifier.startpage599
dc.identifier.endpage602
dc.contributor.firstauthorID2755438


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