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Serum Neurophysins in Familial Central Diabetes Insipidus
The Journal of Clinical Endocrinology & Metabolism, 1978Antibovine neurophysin antibodies (anti-bNpI and/or anti-bNpII) are present in certain patients with familial central diabetes insipidus; these are exogenous origin, as they are not present in patients who have not received treatment with crude posterior pituitary extracts over the years preceding the analysis.
J J, Legros, J, Crabbe
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Central diabetes insipidus: beware of Langerhans cell histiocytosis!
The Netherlands journal of medicine, 2018Langerhans cell histiocytosis (LCH) is a rare disorder, characterised by a monoclonal proliferation of aberrant histiocytes that accumulate in and infiltrate into different organs. When the hypothalamic-pituitary axis is involved, central diabetes insipidus (CDI) can be its first manifestation.
Brys, A D H +4 more
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Central diabetes insipidus in hypoxic brain damage
Child's Nervous System, 1992We describe two children who after cardiopulmonary arrest developed hypernatremia at the terminal stage. Urinary antidiuretic hormone concentration was very low, indicating central diabetes insipidus. These cases illustrate the necessity of alertness to the development of central diabetes insipidus in patients with severe hypoxic brain damage.
O, Arisaka +6 more
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Central diabetes insipidus associated with Caroli syndrome
The Indian Journal of Pediatrics, 2007Caroli disease is a rare congenital malformation characterized by cystic dilatations of large bile ducts. There are two forms of Caroli disease. Simple form entails the bile duct dilatation or ectasia. Complex form is copresense of hepatic fibrosis and portal hypertension.
Semra, Cetinkaya, Ayfer, Alikasifoglu
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Central Diabetes Insipidus Caused by Brain Death
Archives of Pediatrics & Adolescent Medicine, 1986Sir.—The article by Greger et al1describing 73 children with central diabetes insipidus (DI) over 22 years failed to emphasize that one of the most common causes of DI during childhood is brain death. Outwater and I2reported the development of DI in 14 of 16 children who met criteria for brain death over a two-year period.
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[Central diabetes insipidus: diagnostic difficulties].
Annales d'endocrinologie, 2008Central diabetes insipidus is rare in children. Characteristic features include polyuria and polydipsia due to arginine vasopressin deficiency. The differential diagnosis of polyuric states may be difficult. Etiologic diagnosis of central diabetes insipidus may be an equally difficult task.To specify the difficulties encountered in the diagnosis of ...
N, Matoussi +6 more
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