Indication
Partial central diabetes insipidus
Partial central diabetes insipidus, also classified as partial arginine vasopressin deficiency, is an endocrine disorder of water homeostasis affecting children and adults. Read more about Partial central diabetes insipidus
52 drugs 38 manufacturers
Drugs that treat it
Common Partial central diabetes insipidus therapies.
DESMOPRESSIN ACETATE
DESMOPRESSIN (desmopressin acetate)
DESMOPRESSIN (desmopressin acetate)
DESMOPRESSIN ACETATE
DESMOPRESSIN ACETATE
DESMOPRESSIN ACETATE (desmopressin acetate (non-refrigerated))
DESMOPRESSIN (desmopressin acetate)
DDAVP (desmopressin acetate)
News & literature
Coming soonRelated codes
Coming soonRelated conditions & guidelines
Coming soonPartial central diabetes insipidus, also classified as partial arginine vasopressin deficiency, is an endocrine disorder of water homeostasis affecting children and adults.
It is characterized by an incomplete deficiency in the hypothalamic synthesis, transport, or posterior pituitary secretion of antidiuretic hormone (arginine vasopressin), often arising from neurosurgery, head trauma, intracranial neoplasms, infiltrative diseases, or idiopathic causes.
Unlike complete forms, patients retain residual hormone secretion, allowing modest endogenous urinary concentration under osmotic stress.
Consequently, it clinically manifests as variable degrees of hypotonic polyuria, compensatory polydipsia, and an impaired renal ability to conserve free water, with a significant increase in urine osmolality following exogenous vasopressin administration.
- nih.gov
Partial central diabetes insipidus, also classified as partial arginine vasopressin deficiency, is an endocrine disorder of water homeostasis affecting children and adults
- nih.gov
It is characterized by an incomplete deficiency in the hypothalamic synthesis, transport, or posterior pituitary secretion of antidiuretic hormone (arginine vasopressin), often arising from neurosurgery, head trauma, intracranial neoplasms, infiltrative diseases, or idiopathic causes Unlike complete forms, patients retain residual hormone secretion, allowing modest endogenous urinary concentration under osmotic stress Consequently, it clinically manifests as variable degrees of hypotonic polyuri...
- litfl.com
It is characterized by an incomplete deficiency in the hypothalamic synthesis, transport, or posterior pituitary secretion of antidiuretic hormone (arginine vasopressin), often arising from neurosurgery, head trauma, intracranial neoplasms, infiltrative diseases, or idiopathic causes Unlike complete forms, patients retain residual hormone secretion, allowing modest endogenous urinary concentration under osmotic stress
- nih.gov
Consequently, it clinically manifests as variable degrees of hypotonic polyuria, compensatory polydipsia, and an impaired renal ability to conserve free water, with a significant increase in urine osmolality following exogenous vasopressin administration
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