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Hereditary Nephrogenic Diabetes Insipidus Type‐2
Author(s) -
Matsumoto Tohru,
Ito Yuhei,
Yukizane Shigenori,
Ichikawa Kotaro,
Yamashita Fumio
Publication year - 1988
Publication title -
pediatrics international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.49
H-Index - 63
eISSN - 1442-200X
pISSN - 1328-8067
DOI - 10.1111/j.1442-200x.1988.tb02559.x
Subject(s) - nephrogenic diabetes insipidus , medicine , in utero , antidiuretic , amniotic fluid , diabetes insipidus , endocrinology , fetus , pregnancy , hormone , biology , genetics
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.