Results 21 to 30 of about 1,174 (110)
Late onset of familial neurogenic diabetes insipidus in monozygotic twins
Endocrine Regulations, 2013 Autosomal dominant familial diabetes insipidus (FNDI) is a rare disease characterized by polydipsia and polyuria due to deficiency of the antidiuretic hormone, arginine vasopressin (AVP). We report the first Slovak family with the disease. Noteworthy is the concordantly belated debut of the disease symptoms in two monozygotic twin proband girls in the ...
M, Cizmarova +6 more
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Neurogenic diabetes insipidus in patients with systemic lupus erythematosus
Annals of the Rheumatic Diseases, 1998 Neurogenic diabetes insipidus (NDI) approximately affects one of 25 000 people. The idiopathic type represents about 30% of all NDI cases (one of 75 000).1 The coexistence of primary NDI and systemic lupus erythematosus (SLE) is an exceptional fact that has not been previously described.
JULIO SÁNCHEZ-ROMÁN +4 more
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Central Neurogenic Diabetes Insipidus, Syndrome of Inappropriate Secretion of Antidiuretic Hormone, and Cerebral Salt-Wasting Syndrome in Traumatic Brain Injury [PDF]
Critical Care Nurse, 2012 Central neurogenic diabetes insipidus, syndrome of inappropriate secretion of antidiuretic hormone, and cerebral salt-wasting syndrome are secondary events that affect patients with traumatic brain injury. All 3 syndromes affect both sodium and water balance; however, they have differences in pathophysiology, diagnosis, and treatment.
Cynthia A, John, Michael W, Day
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A Rare Case of Central Diabetes Insipidus in a Pediatric Patient
Acta Médica PortuguesaN/a.
Ana Raquel Henriques +4 more
doaj +1 more source
A Case report of Wolfram Syndrome
مجله دانشگاه علوم پزشکی بیرجند, 2013 Wolfram Syndrome is a neurodegenerative autosomal recessive disorder. The occurrence of the disease should be suspected if non-autoimmune insulin-dependent diabetes occurs in an under-sixteen year old person having bilateral optic nerve atrophy. Diabetes
Samaneh Norooziasl +1 more
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Advances in Research, 2023 To report and review a case of prolactin-producing pituitary tumor presenting with mass effects, hormonal deficiency, and neurogenic diabetes insipidus in a nulliparous woman of Afro-Caribbean descent. The patient presented with dull-aching headaches associated with worsening vision, nausea, and vomiting.
Adedeji Okikiade +5 more
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São Paulo Medical JournalCONTEXT: Central diabetes insipidus (CDI) is a rare cause of hypernatremia during the neonatal period. The diagnosis is particularly difficult in very low birth weight (VLBW) newborns.
Maria Lúcia Silveira Ferlin +3 more
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Journal of Ophthalmic & Vision Research, 2010 Purpose: To report a case of Wolfram syndrome characterized by early onset diabetes mellitus and progressive optic atrophy. Case Report: A 20-year-old male patient with diabetes mellitus type I presented with best corrected visual acuity of 1/10 in both
Gholamali Naderian +3 more
doaj
Polydipsia and polyuria for nine years, unsteady gait and slurred speech for one year
Chinese Journal of Contemporary Neurology and Neurosurgery, 2015 DOI: 10.3969/j.issn.1672-6731.2015.08 ...
Fei-fei ZHAI +4 more
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Problems of Endocrinology, 2003 Fifty two patients (23 males and 29 females) with neurogenic diabetes insipidus (DI) were examined to define the role and specific features of brain magnetic resonance imaging (MRI) in the diagnosis of hypothalamopituitary abnormalities in this disease retrospectively after establishing the diagnosis.
I. I. Dedov +5 more
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