Autosomal Dominant Neurohypophyseal Diabetes Insipidus in Two Families
Background: Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI) is a rare disease with symptoms of polydipsia, polyuria and dehydration caused by arginine vasopressin deficiency. Disease onset is within infancy or adolescence. A variety of disease-causing mutations of the argini...
Main Authors: | , , , , , , , |
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Other Authors: | |
Format: | Article |
Language: | English |
Published: |
Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden
2014
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Online Access: | http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-134493 http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-134493 http://www.qucosa.de/fileadmin/data/qucosa/documents/13449/HRE2009071002111.PDF |