Skip to main content
Log in

Hyperaminoaciduria in childhood

  • For General Practitioners
  • Published:
The Indian Journal of Pediatrics Aims and scope Submit manuscript

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

References

  • Allan, J. D., Cusworth D. C., Dent, C. E. and Wilson, V. K. (1958). Disease, probably hereditary, characterised by severe mental deficiency and a constant gross abnormality of aminoacid metabolism.Lancet,1, 182.

    Article  PubMed  CAS  Google Scholar 

  • Andrews, B. F., Burton, C. O. and Baare, L., (1962). Serum aminoacid nitrogen in infancy and childhood.J. Pediat. 60, 201.

    Article  PubMed  CAS  Google Scholar 

  • Baron, D. N., Dent, C. F., Harris, H., Hart, E. W. and Jepson, J. B. (1956). Hereditary pellagra-like skinrash with temporary cerebellar ataxia, constant renal aminoaciduria and other bizarre biochemical features.Lancet,2, 421.

    Article  Google Scholar 

  • Bearn, A. G., Yu, T. and Gutman A. (1957). Renal function in Wilson’s disease.J. clin. Invest. 36, 1107.

    PubMed  CAS  Google Scholar 

  • Berry, H. K. (1960). Urinary excretion of aminoacids in normal infants and children.Pediatrics,6, 983.

    Google Scholar 

  • Chaudhuri, Amala, Nag Chaudhuri, J. and Chaudhuri, K. C. (1960). Infantile cirrhosis.J. Pediat. 57, 230.

    Article  PubMed  CAS  Google Scholar 

  • Cheung, M. W., Fowler, D. I., Norton, P. M., Snyderman, S. E. and Holt, L. E. Jr. (1955). Observations on aminoacid metabolism in kwashiorkor.J. trop. Pediat. 1, 141.

    Google Scholar 

  • Childs, B. (1952). Urinary excretion of free alpha amino nitrogen by normal infants and children.Proc. Soc. exp. Bio. Med. 81, 225.

    CAS  Google Scholar 

  • Childs, B., Nyhan, W., Borden, M., Bard, L. and Cooke, R. E., (1961). Idiopathic hyperglycinemia and hyperglycinuria. A new disorder of aminoacid metabolism.Pediatrics,27, 522.

    PubMed  CAS  Google Scholar 

  • Chisolm, J. J. Jr., and Harrison, H. E. (1962). Aminoaciduria in vitamin D deficiency states in premature infants and older children with rickets.J. Pediat. 60, 206.

    Article  PubMed  Google Scholar 

  • Chowers, I., Czackes, J. W., Ehrenfeld, E. N. and Landau, Suzan. (1962). Familial aminoaciduria in osteogenesis imperfecta.J. Amer. med. Ass. 181, 7.

    Google Scholar 

  • Clay, R. D., Darmody, E. M. and Hawkins, M. (1953). Nature of the renal lesion in Fanconi syndrome.J. Path. Bact. 65, 551.

    Article  PubMed  CAS  Google Scholar 

  • Cusworth, D. C., Dent, C. E. and Flynn, F. V. (1953). The aminoaciduria in galactosemia.Arch. Dis. Childh. 30, 150.

    Article  Google Scholar 

  • Dent, C. E. and Walsh, J. M. (1954). Aminoacid metabolism.Brit. med. Bull. 10, 247.

    PubMed  CAS  Google Scholar 

  • Dent, C. E. and Rose, G. (1951). Aminoacid metabolism in cystinuria.Quart. J. Med.,20, 205.

    PubMed  CAS  Google Scholar 

  • Dent, C. E. and Westal, R. G. (1961). Studies in maple syrup urine disease.Arch. Dis. Childh. 36, 259.

    PubMed  CAS  Google Scholar 

  • De Vries, A. Kochwa, S., Lazebnik, J., Frank, M., and Djaldetti, M., (1957). Glycinuria a hereditary disorder associated with nephrolithiasis.Amer. J. Med.,23, 408.

    Article  Google Scholar 

  • Doolan, P. D.et al. (1955). Renal clearance of eighteen individual aminoacids in human subjects.J. clin. Invest. 34, 1247.

    PubMed  CAS  Google Scholar 

  • Dunn, M. S., Akawie, S., Yeh, H. L. and Martin, H. (1950). Urinary excretion of aminoacids in liver disease.J. clin. Invest. 29, 302.

    PubMed  CAS  Google Scholar 

  • Dustin, J. P. and Bigwood, E. J. (1954). Aminoaciduria in infancy and ascorbic acid deficiency.Proc. nutr. Soc. 12, 233.

    CAS  Google Scholar 

  • Dustin, J. P., Moore, S. and Bigwood, E. J. (1955). Chromatographic studies on excretion of aminoacids in early infancy.Metabolism,4, 75.

    PubMed  CAS  Google Scholar 

  • Ghadami, H. and Shwachman, H. (1960). Evaluation of aminoaciduria in infancy and childhood.Amer. J. Dis. Child. 99, 947.

    Google Scholar 

  • Ghadami, H., Partington, M. W. and Hunter, A. (1961). A familial disturbance of histidine metabolism.New Engl. J. Med. 265, 221.

    Article  Google Scholar 

  • Harper, H. A. (1961). Review of physiological chemistry, 6th Ed.Lange, Los Angeles.

    Google Scholar 

  • Harris, H., Penrose, S. and Thomas, D. H. (1959) Cystathioninuria.Ann. Human Genet. 23, 442.

    Article  CAS  Google Scholar 

  • Hurley, K. E. and Williams, R. J. (1955). Urinary aminoacids, creatinine and phosphate in muscular dystrophy.Arch. Biochem. 54, 384.

    Article  PubMed  CAS  Google Scholar 

  • Ingle, V. N. Unpublished data.

  • Isselbacher, K. J., Anderson, E. P., Kurahashi, K. and Kackar, H. M. (1956). Congenital galactosemia, a single enzymatic block in galactose metabolism.Science,123, 635.

    Article  PubMed  CAS  Google Scholar 

  • Jagenburg, O. R. (1959). The urinary excretion of free aminoacids and other compounds.Scand. J. Clin. & Lab. Invest. 2, Suppl. 43.

    Google Scholar 

  • Jervis, G. A. (1950). Excretion of phenylalanine and derivatives in phenylpyruvic oligophrenia.Proc. Soc. exper. Bio. Med. 75, 83.

    CAS  Google Scholar 

  • Idem, (1953). Phenylpyruvic oligophrenia, a deficiency of phenylalanine oxidizing system.Ibid.82, 51.

    Google Scholar 

  • Joxin, J. H. P. and Huisman, T. H. J. (1953). Aminoaciduria in rachitic children.Lancet,2, 428.

    Google Scholar 

  • Joxin, J. H. P. and Huisman, T. H. J. (1954). Aminoaciduria in ascorbic acid deficiency.Pediatrics,14, 238.

    Google Scholar 

  • Knox, W. E. (1960). An evaluation of the treatment of phenylketonurics with diets low in phenylalanine.Pediatrics,26, 1.

    PubMed  CAS  Google Scholar 

  • Levine, B. Mackay, H. M., and Oberholzer, V. G. (1961). Arginosuccinic aciduria.Arch. Dis. Childh. 36, 622.

    Article  Google Scholar 

  • Lowe, C. U., Terry, M. and MacLachlan, E. A. (1952). Organic amino-aciduria, decreased renal ammonia production hydrophthalmos and mental retardation.Amer. J. Dis. Child. 83, 164.

    CAS  Google Scholar 

  • MacMurray, W. C., Rathburn, J. C., Mohyuddin, F. and Joegner, S. (1963). Citrillinuria.Pediatrics,32, 347.

    Google Scholar 

  • Mehta, S., Walia, B. N. S., Ghai, O. P. and Taneja, P. N. (1964). A qualitative study of plasma and urinary aminoacids in Indian childhood cirrhosis.Indian J. Pediat. 31, 187.

    PubMed  CAS  Google Scholar 

  • Mackenzie, D. N. and Woolf, L. I., (1959). Maple syrup urine disease.Brit. med. J. 1, 90.

    PubMed  CAS  Google Scholar 

  • Menkes, J. H. (1959). Maple syrup disease —isolation and identification of organic acids in the urine.Neurology,9, 826.

    Google Scholar 

  • Parry, T. E. (1959). Aminoaciduria in liver disease.Arch. Dis. Childh. 174, 188.

    Google Scholar 

  • Rose, G. A. (1959). Cystinuria.Lancet,1, 780.

    Google Scholar 

  • Rothstein, A. and Berke, H. (1949). Aminoaciduria in uranium poisoning.J. Pharmacol. and Exper. Therap. 96, 179.

    CAS  Google Scholar 

  • Sass Kartsak, Chernia, M., Greiger, D. W. and Slater, R. J. (1959). Observations on ceruloplasmin in Wilson’s disease.J. Clin. Invest. 38, 1672.

    Google Scholar 

  • Scheinberg, A. H. and Gitlin, D. (1952). Deficiency of ceruloplasmin in patients with hepatclenticular degeneration (Wilson’s disease).Science,116, 484.

    Article  PubMed  CAS  Google Scholar 

  • Schafer, I. A., Scriver, C. and Efron, M. L. (1961). Multiple congenital anomalies in a family with an error in proline metabolism.Amer. J. Dis. Child. 102, 632.

    Google Scholar 

  • Schonenberg, H. (1954). Quoted by Synderman, S. E.

    Google Scholar 

  • Synderman, S. E., Dancies, J., Norten, P. M. and Holt, L. E. Jr. (1960). The treatment of a case of maple syrup urine disease.Amer. J. Dis. Child. 100, 633.

    Google Scholar 

  • Steinberg, A. H., Steinberg, A. and Cohen, N. E. (1957). Aminoaciduria and hypermetabolism in progeria.Arch. Dis. Child. 32, 401.

    PubMed  CAS  Google Scholar 

  • Stein, W. H., Bearn, A. G. and Moore, S. (1954). The aminoacid content of the blood and urine and Wilson’s disease.J. clin. Invest. 33, 410.

    PubMed  CAS  Google Scholar 

  • Thelander, H. E. and Imagawa, R. (1956). Aminoaciduria, congenital defects and mental retardation, a preliminary report.J. Pediat. 49, 123.

    Article  PubMed  CAS  Google Scholar 

  • Their, S., Fox, M., Segal, S., and Rosenberg, L. E. (1964). Cystinuria,In vitro demonstration of an intestinal transport defect.Science,143, 482.

    Article  Google Scholar 

  • Uzman, L. L. and Hood, B. (1952). Familial nature of the aminoaciduria of Wilson’s disease (hepatolenticular degeneration).Amer. J. Med. Sc. 223, 392.

    Article  CAS  Google Scholar 

  • Wilson, V. K., Thomson, M. L., and Dent, C. E. (1953). Aminoaciduria in lead poisoning.Lancet,2, 66.

    Article  Google Scholar 

  • Woolf, L. I. and Giles, H. M. (1956). Urinary excretion of aminoacids and sugar in nephrotic syndrome.Acta Pediat. 45, 489.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

From the Department of Pediatrics, Medical College, Aurangabad.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ingle, V.N. Hyperaminoaciduria in childhood. Indian J Pediatr 33, 56–62 (1966). https://doi.org/10.1007/BF02803758

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02803758

Keywords

Navigation