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Vasopressin-Resistant Diabetes Insipidus

Vasopressin-Resistant Diabetes Insipidus Abstract In 1947 Williams and Henry1 introduced the term "nephrogenic" to describe a form of diabetes insipidus in patients whose symptoms were not relieved by the administration of vasopressin. The disease had been mentioned in 1923 by Veil,2 who noted the same lack of response in some of his patients. The published literature until 1945 describing this type of diabetes insipidus (as well as the ordinary type in which vasopressin is effective) was reviewed by Forssman,3 who also included eight cases of his own. The supposition that the kidney was at fault was made by Williams and Henry1 on the basis that renal function was found to be somewhat impaired in the patient whom they studied. They found the renal plasma flow (R. P. F.), the maximal tubular excretion (Tm) of iodopyracet (Diodrast), and the urea clearance to be low, in addition to subnormal renal concentrating powers References 1. Williams, R. H., and Henry C.: Nephrogenic Diabetes Insipidus transmitted by Females and Appearing During Infancy in Males , Ann. Int. Med. 27:84, 1947.Crossref 2. Veil, W. H.: Physiologie und Pathologie des Wasserhaushaltes , Ergebn. inn. Med. u. Kinderh. 23:648, 1923. 3. Forssman, H.: On Hereditary Diabetes Insipidus with Special Regard to a Sex-Linked Form , Acta med. scandinav. Supp. 159:1, 1945. 4. Waring, A. J.; Kajdi, L., and Tappan, V.: A Congenital Defect of Water Metabolism , Am. J. Dis. Child. 69:323, 1945. 5. Dancis, J.; Birmingham, J. R., and Leslie, S. H.: Congenital Diabetes Insipidus Resistant to Treatment with Pitressin , Am. J. Dis. Child. 75:316, 1948. 6. MacDonald, W. B.: Congenital Nephrogenic Diabetes Insipidus , M. J. Australia 2:32, 1953. 7. Kao, M. Y. C., and Steiner, M. M.: Diabetes Insipidus in Infancy Resistant to Pitressin , Pediatrics 12:400, 1953. 8. Guard, H. L.: Pitressin Resistant Diabetes Insipidus: Nephrogenic Function Defect; Report of Case , M. Bull. U. S. Army Europe 10:185, 1953. 9. Luder, J., and Burnett, D.: A Congenital Renal Tubular Defect , Arch. Dis. Childhood 29: 44, 1954.Crossref 10. MacDonald, W. B.: Congenital Pitressin Resistant Diabetes Insipidus of Renal Origin , Pediatrics 15:298, 1955. 11. West, J. R., and Kramer, J. G.: Nephrogenic Diabetes Insipidus , Pediatrics 15:424, 1955. 12. Maggi, R.; Garcia Diaz, C. J., and Vecchio, H.: Diabetes insipida resistente al Pitressin en un niño de años , Semana méd. 106:1, 1955. 13. Gautier, E., and Prader, A.: Un Cas de diabete insipide nephrogene chez un nourrisson, avec absence initiale de soif (diabete insipide occulte) , Helvet. paediat. acta 11:1, 1956. 14. Hillman, D. A.; Neyzi, O.; Porter, P.; Cushman, A., and Talbot, N. B.: Renal (Vasopressin-Resistant) Diabetes Insipidus , Pediatrics 21: 430, 1958. 15. Kirman, B.; Black, J. A.; Wilkinson, R. H., and Evans, P. R.: Familial Pitressin-Resistant Diabetes Insipidus with Mental Defect , Arch. Dis. Childhood 31:59, 1956.Crossref 16. Ellborg, A., and Forssman, H.: Nephrogenic Diabetes Insipidus in Children , Acta paediat. 44: 209, 1955.Crossref 17. Boer, M. A.: Nephrogenic Diabetes Insipidus, Kinderklin. report , Maandschr. kindergeneesk . 24:204, 1956. 18. Walker, N. F., and Rance, C. P.: Inheritance of Nephrogenic Diabetes Insipidus , Am. J. Human Genet. 6:354, 1954. 19. Forssman, H.: Form of Diabetes Insipidus Characterized by Sex-Linked Inheritance and Unresponsiveness to the Antidiuretic Hormone: New Genotypic Entity , Acta endocrinol. 16:355, 1954. 20. Cannon, J. F.: Diabetes Insipidus , A. M. A. Arch. Int. Med. 96:215, 1955.Crossref 21. Carter, C., and Simpkiss, M.: The Carrier State in Nephrogenic Diabetes Insipidus , Lancet 2:1069, 1956.Crossref 22. Jonxis, J. H., and Huisman, T. H.: The Renal Element in Rachitic Amino-Aciduria , Lancet 2:513, 1954.Crossref 23. Jonxis, J. H., and Huisman, T. H.: Amino Aciduria in Ascorbic Acid Deficiency , Pediatrics 14:238, 1954. 24. Lathem, W.; Baker, K., and Bradley, E. S.: Urinary Amino Acid Excretion in Renal Disease with Observations on the Fanconi Syndrome , Am. J. Med. 18:249, 1955.Crossref 25. Kaplan, S. A.; Yuceoglu, A. M., and Strauss, J.: Unpublished observations. 26. Wilkins, L.: The Diagnosis and Treatment of Endocrine Disorders in Childhood and Adolescence , Ed. 2, Springfield, Ill., Charles C Thomas, Publisher, 1957. 27. Brodsky, W. A., and Rapoport, S.: The Mechanism of Polyuria of Diabetes Insipidus in Man , J. Clin. Invest. 30:282, 1951.Crossref http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png A.M.A. Journal of Diseases of Children American Medical Association

Vasopressin-Resistant Diabetes Insipidus

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American Medical Association
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Copyright © 1959 American Medical Association. All Rights Reserved.
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0096-6916
DOI
10.1001/archpedi.1959.02070010310008
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Abstract

Abstract In 1947 Williams and Henry1 introduced the term "nephrogenic" to describe a form of diabetes insipidus in patients whose symptoms were not relieved by the administration of vasopressin. The disease had been mentioned in 1923 by Veil,2 who noted the same lack of response in some of his patients. The published literature until 1945 describing this type of diabetes insipidus (as well as the ordinary type in which vasopressin is effective) was reviewed by Forssman,3 who also included eight cases of his own. The supposition that the kidney was at fault was made by Williams and Henry1 on the basis that renal function was found to be somewhat impaired in the patient whom they studied. They found the renal plasma flow (R. P. F.), the maximal tubular excretion (Tm) of iodopyracet (Diodrast), and the urea clearance to be low, in addition to subnormal renal concentrating powers References 1. Williams, R. H., and Henry C.: Nephrogenic Diabetes Insipidus transmitted by Females and Appearing During Infancy in Males , Ann. Int. Med. 27:84, 1947.Crossref 2. Veil, W. H.: Physiologie und Pathologie des Wasserhaushaltes , Ergebn. inn. Med. u. Kinderh. 23:648, 1923. 3. Forssman, H.: On Hereditary Diabetes Insipidus with Special Regard to a Sex-Linked Form , Acta med. scandinav. Supp. 159:1, 1945. 4. Waring, A. J.; Kajdi, L., and Tappan, V.: A Congenital Defect of Water Metabolism , Am. J. Dis. Child. 69:323, 1945. 5. Dancis, J.; Birmingham, J. R., and Leslie, S. H.: Congenital Diabetes Insipidus Resistant to Treatment with Pitressin , Am. J. Dis. Child. 75:316, 1948. 6. MacDonald, W. B.: Congenital Nephrogenic Diabetes Insipidus , M. J. Australia 2:32, 1953. 7. Kao, M. Y. C., and Steiner, M. M.: Diabetes Insipidus in Infancy Resistant to Pitressin , Pediatrics 12:400, 1953. 8. Guard, H. L.: Pitressin Resistant Diabetes Insipidus: Nephrogenic Function Defect; Report of Case , M. Bull. U. S. Army Europe 10:185, 1953. 9. Luder, J., and Burnett, D.: A Congenital Renal Tubular Defect , Arch. Dis. Childhood 29: 44, 1954.Crossref 10. MacDonald, W. B.: Congenital Pitressin Resistant Diabetes Insipidus of Renal Origin , Pediatrics 15:298, 1955. 11. West, J. R., and Kramer, J. G.: Nephrogenic Diabetes Insipidus , Pediatrics 15:424, 1955. 12. Maggi, R.; Garcia Diaz, C. J., and Vecchio, H.: Diabetes insipida resistente al Pitressin en un niño de años , Semana méd. 106:1, 1955. 13. Gautier, E., and Prader, A.: Un Cas de diabete insipide nephrogene chez un nourrisson, avec absence initiale de soif (diabete insipide occulte) , Helvet. paediat. acta 11:1, 1956. 14. Hillman, D. A.; Neyzi, O.; Porter, P.; Cushman, A., and Talbot, N. B.: Renal (Vasopressin-Resistant) Diabetes Insipidus , Pediatrics 21: 430, 1958. 15. Kirman, B.; Black, J. A.; Wilkinson, R. H., and Evans, P. R.: Familial Pitressin-Resistant Diabetes Insipidus with Mental Defect , Arch. Dis. Childhood 31:59, 1956.Crossref 16. Ellborg, A., and Forssman, H.: Nephrogenic Diabetes Insipidus in Children , Acta paediat. 44: 209, 1955.Crossref 17. Boer, M. A.: Nephrogenic Diabetes Insipidus, Kinderklin. report , Maandschr. kindergeneesk . 24:204, 1956. 18. Walker, N. F., and Rance, C. P.: Inheritance of Nephrogenic Diabetes Insipidus , Am. J. Human Genet. 6:354, 1954. 19. Forssman, H.: Form of Diabetes Insipidus Characterized by Sex-Linked Inheritance and Unresponsiveness to the Antidiuretic Hormone: New Genotypic Entity , Acta endocrinol. 16:355, 1954. 20. Cannon, J. F.: Diabetes Insipidus , A. M. A. Arch. Int. Med. 96:215, 1955.Crossref 21. Carter, C., and Simpkiss, M.: The Carrier State in Nephrogenic Diabetes Insipidus , Lancet 2:1069, 1956.Crossref 22. Jonxis, J. H., and Huisman, T. H.: The Renal Element in Rachitic Amino-Aciduria , Lancet 2:513, 1954.Crossref 23. Jonxis, J. H., and Huisman, T. H.: Amino Aciduria in Ascorbic Acid Deficiency , Pediatrics 14:238, 1954. 24. Lathem, W.; Baker, K., and Bradley, E. S.: Urinary Amino Acid Excretion in Renal Disease with Observations on the Fanconi Syndrome , Am. J. Med. 18:249, 1955.Crossref 25. Kaplan, S. A.; Yuceoglu, A. M., and Strauss, J.: Unpublished observations. 26. Wilkins, L.: The Diagnosis and Treatment of Endocrine Disorders in Childhood and Adolescence , Ed. 2, Springfield, Ill., Charles C Thomas, Publisher, 1957. 27. Brodsky, W. A., and Rapoport, S.: The Mechanism of Polyuria of Diabetes Insipidus in Man , J. Clin. Invest. 30:282, 1951.Crossref

Journal

A.M.A. Journal of Diseases of Children – American Medical Association

Published: Mar 1, 1959

References

  • Nephrogenic Diabetes Insipidus transmitted by Females and Appearing During Infancy in Males
    Williams , R. H., and Henry C.
  • Physiologie und Pathologie des Wasserhaushaltes
    Veil , W. H.
  • On Hereditary Diabetes Insipidus with Special Regard to a Sex-Linked Form
    Forssman , H.
  • A Congenital Defect of Water Metabolism
    Waring , A. J.; Kajdi, L., and Tappan, V.
  • Congenital Diabetes Insipidus Resistant to Treatment with Pitressin
    Dancis , J.; Birmingham, J. R., and Leslie, S. H.
  • Congenital Nephrogenic Diabetes Insipidus
    MacDonald , W. B.
  • Diabetes Insipidus in Infancy Resistant to Pitressin
    Kao , M. Y. C., and Steiner, M. M.
  • Pitressin Resistant Diabetes Insipidus: Nephrogenic Function Defect
    Guard , H. L.
  • A Congenital Renal Tubular Defect
    Luder , J., and Burnett, D.
  • Congenital Pitressin Resistant Diabetes Insipidus of Renal Origin
    MacDonald , W. B.
  • Nephrogenic Diabetes Insipidus
    West , J. R., and Kramer, J. G.
  • Diabetes insipida resistente al Pitressin en un niño de años
    Maggi , R.; Garcia Diaz, C. J., and Vecchio, H.
  • Un Cas de diabete insipide nephrogene chez un nourrisson, avec absence initiale de soif (diabete insipide occulte)
    Gautier , E., and Prader, A.
  • Renal (Vasopressin-Resistant) Diabetes Insipidus
    Hillman , D. A.; Neyzi, O.; Porter, P.; Cushman, A., and Talbot, N. B.
  • Familial Pitressin-Resistant Diabetes Insipidus with Mental Defect
    Kirman , B.; Black, J. A.; Wilkinson, R. H., and Evans, P. R.
  • Nephrogenic Diabetes Insipidus in Children
    Ellborg , A., and Forssman, H.
  • Nephrogenic Diabetes Insipidus, Kinderklin. report
    Boer , M. A.
  • Inheritance of Nephrogenic Diabetes Insipidus
    Walker , N. F., and Rance, C. P.
  • Form of Diabetes Insipidus Characterized by Sex-Linked Inheritance and Unresponsiveness to the Antidiuretic Hormone: New Genotypic Entity
    Forssman , H.
  • Diabetes Insipidus
    Cannon , J. F.
  • The Carrier State in Nephrogenic Diabetes Insipidus
    Carter , C., and Simpkiss, M.
  • The Renal Element in Rachitic Amino-Aciduria
    Jonxis , J. H., and Huisman, T. H.
  • Amino Aciduria in Ascorbic Acid Deficiency
    Jonxis , J. H., and Huisman, T. H.
  • Urinary Amino Acid Excretion in Renal Disease with Observations on the Fanconi Syndrome
    Lathem , W.; Baker, K., and Bradley, E. S.
  • The Diagnosis and Treatment of Endocrine Disorders in Childhood and Adolescence
    Wilkins , L.
  • The Mechanism of Polyuria of Diabetes Insipidus in Man
    Brodsky , W. A., and Rapoport, S.