Dietary Management of Inborn Errors of Metabolism

Indian Journal of Pediatrics

Volumn 69, Issue 5, 2002, Pages 421-426

  Kabra, Madhulika ^a  

^a ALL INDIA INSTITUTE OF MEDICAL SCIENCES   (India)

Author keywords

Dietary management; Inborn errors of metabolism; Indian modifications

Indexed keywords

CHILD; DIET THERAPY; GALACTOSEMIA; GLYCOGEN STORAGE DISEASE; HOMOCYSTINURIA; HUMAN; INBORN ERROR OF METABOLISM; MAPLE SYRUP URINE DISEASE; METHODOLOGY; PHENYLKETONURIA; REVIEW;

CHILD; DIET THERAPY; GALACTOSEMIAS; GLYCOGEN STORAGE DISEASE; HOMOCYSTINURIA; HUMANS; MAPLE SYRUP URINE DISEASE; METABOLISM, INBORN ERRORS; PHENYLKETONURIAS;

EID: 0036580578     PISSN: 00195456     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02722635     Document Type: Conference Paper

References (12)

1. Council of Europe report 1973.
2. ICMR Collaborating Centres and Central Co-ordinating Unit. Multricentric study on genetic causes of mental retardation in India. Indian J Med Res 1991; 94 : 161-169.
3. Ambani LM, Patel ZM, Dhareshwar SS et al. Clinical, biochemical and cytogenetic studies in mental retardation. Indian J Med Res 1984; 79 : 384-387.
4. Kaur M, Das GP, Verma IC. Inborn errors of aminoacid metabolism in North India. J Inherit Metab Dis 1994; 17 : 1-4.
5. Dietary management of disorders of aminoacid metabolism, organic acduria and urea cycle defects. Diets for Sick Children. 1987. 263-312, Dorothy Em Francis 4th edn. Blackwell Scientific Publications.
6. Phenylketonuria in dietary management of disorders of aminoacid metabolism, organic aciduria and urea cycle defects. Diets for Sick Children. 224-262, 1987; Dorothy Em Francis. 4th edn. Blackwell Scientific Publications.
7. Patel ZM, Bajaj RT, Ambani LM. Dietary therapy of Inborn errors of metabolism in India with special reference to phenylketonuria. In Verma IC, ed. Genetic Research in India. Sagar Publishers 1986; 150-152,
8. Kaur M, Kabra M, Das GP et al. Clinical and biochemical studies in homocystinuria. Indian Pediatr 1995; 32 : 1067-1075.
9. Brandt NJ. How long should galactossemia be treated ? Burman D, Helten JB, Pennock CA, eds. Inherited Disorders of Carbohydrate Metabolism. Lancaster MTP press Ltd., 1980; 117-124.
10. Gitzelmann R, Auricchio S. Handling of soya or galactosides by a normal and galactossemia child. Pediatrics 1965; 36 : 231.
11. Clotheir CM, Davidson DC. Galactossemia workshop. Hum Nutr Appl Nutr 1983; 37A : 483-490.
12. Chen YT, Bazzarre CH, Lee MM et al. Type I glycogen storage disease: Nine years of management with corn starch. Eur J Pediatr 1993; 152-556.