EARLY-ONSET CENTRAL DIABETES INSIPIDUS IN A NEWBORN WITH HOLOPROSENCEPHALY

Aslan, Mustafa; Ince, Elmas; Coban, Asuman

doi:10.26650/iuitfd.2021.807168

EARLY-ONSET CENTRAL DIABETES INSIPIDUS IN A NEWBORN WITH HOLOPROSENCEPHALY

Atıf İçin Kopyala

Aslan M. T., Ince E., Coban A.

JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI, cilt.84, sa.4, ss.599-602, 2021 (ESCI)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 84 Sayı: 4
Basım Tarihi: 2021
Doi Numarası: 10.26650/iuitfd.2021.807168
Dergi Adı: JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI
Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), TR DİZİN (ULAKBİM)
Sayfa Sayıları: ss.599-602
Anahtar Kelimeler: Holoprosencephaly, central diabetes insipidus, newborn, desmopressin, ORAL DESMOPRESSIN
İstanbul Üniversitesi Adresli: Evet

Özet

Holoprosencephaly 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.