diabetes insipidus centrálny diabetes insipidus, kraniálny typ diabetes insipidus centrálny primárny diabetes insipidus sekundárny, z nedostatku vazopresínu diabetes insipidus neurohypofyzárny diabetes insipidus, neurohypofyzárny typ diabetes insipidus neurohypofýzový diabetes insipidus, neurohypofýzový typ diabetes insipidus hypofýzový diabetes insipidus primárny centrálny nedostatok vazopresínu deficit vazopresínu deficiencia vazopresínu
Scope note in English
A genetic or acquired polyuric disorder caused by a deficiency of VASOPRESSINS secreted by the NEUROHYPOPHYSIS. Clinical signs include the excretion of large volumes of dilute URINE; HYPERNATREMIA; THIRST; and polydipsia. Etiologies include HEAD TRAUMA; surgeries and diseases involving the HYPOTHALAMUS and the PITUITARY GLAND. This disorder may also be caused by mutations of genes such as ARVP encoding vasopressin and its corresponding neurophysin (NEUROPHYSINS).
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