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Hereditary Nephrogenic Diabetes Insipidus Type-2 |
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| Authors: | Tohru Matsumoto M.D. Yuhei Ito M.D. Shigenori Yukizane M.D. Kotaro Ichikawa M.D. Fumio Yamashita M.D. |
| Affiliation: | Department of Pediatrics and Child Health, Kurume University School of Medicine, Kurume;Department of Pediatrics, Yahata Medical Center, Kitakyushu Municipal Hospital Kitakyushu;Chairman of Department of Pediatrics and Child Health, Kurume University School of Medicine, Kurume |
| Abstract: | Nephrogenic diabetes insipidus (NDI) in a fetus in utero was suspected because of the family history, and evidence of increased amniotic fluid by echosonography. The mother's karyo-type was 46 XX/47 XXX. After birth, the patient was diagnosed as NDI type-2 which is partially resistant to antidiuretic hormone. |
| Keywords: | Hereditary nephrogenic diabetes Amniotic fluid Prenatal diagnosis Echosonography |