Chronic Hypernatremia Associated with Holoprosencephaly
نویسندگان
چکیده
منابع مشابه
A Rare Association: Recurrent Hypernatremia, Cleft Lip/palate, and Holoprosencephaly
We report a female infant with facial dysmorphism, ectrodactyly, holoprosencephaly, and associated hypernatremia. A 7-month-old female infant with cleft lip and palate, and ectrodactyly was admitted to our hospital with recurrent hypernatremic dehydration. Magnetic resonance imaging revealed holoprosencephaly. Plasma osmolality was increased whereas urinary osmolality was decreased. Serum ADH l...
متن کاملAlobar holoprosencephaly associated with cebocephaly and craniosynostosis.
Cebocephaly is a very rare congenital midline facial anomaly characterized by a blind-ended single nostril and ocular hypotelorism, and is usually combined with alobar holoprosencephaly. We report here a case of alobar holoprosencephaly with cebocephaly and craniosynostosis. Chromosomal analysis revealed normal karyotyping. The facial dysmorphism was characterized by the single nostril, hypotel...
متن کاملPrevalence of Breastfeeding–associated Hypernatremia among Hospitalized Hyperbilirubinemic Neonates
Introduction: This study aimed to assess the incidence of breastfeeding-associated hypernatremia and related risk factors among hospitalized hyperbilirubinemic neonates. Methods: This prospective study was conducted at Nemazee Hospital affiliated to Shiraz University of Medical Sciences during one year to determine the association between hypernatremia (serum sodium concentration of >150 mEq/L)...
متن کاملUndercorrection of hypernatremia is frequent and associated with mortality
BACKGROUND About 1% of patients admitted to the Emergency Department (ED) have hypernatremia, a condition associated with a mortality rate of 20 to 60%. Management recommendations originate from intensive care unit studies, in which patients and medical diseases differ from those in ED. METHODS We retrospectively studied clinical characteristics, treatments, and outcomes of severely hypernatr...
متن کاملSeptopreoptic holoprosencephaly: a mild subtype associated with midline craniofacial anomalies.
SUMMARY HPE is a congenital brain malformation characterized by failure of the prosencephalon to divide into 2 hemispheres. We have identified 7 patients who have a mild subtype of HPE in which the midline fusion was restricted to the septal region or preoptic region of the telencephalon. This subtype, which we call septopreoptic HPE, falls in the spectrum of lobar HPE, but lacks significant fr...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: The Tohoku Journal of Experimental Medicine
سال: 1979
ISSN: 0040-8727,1349-3329
DOI: 10.1620/tjem.128.333