Anderson's disease (steatorea due to retention of chylomicrons): Diagnostic criteria;Enfermedad de Anderson (esteatorrea por retencion de quilomicrones): Criterios diagnosticos

Anales Espanoles de Pediatria

Volumn 47, Issue 2, 1997, Pages 195-198

  Oltra Benavent, M ^a   Chirivella Casanova, M ^a   Pereda Perez A ^a   Ribes Konickx, C ^a   Ferrer Calvete, J ^a,b  

^a HOSPITAL UNIVERSITARIO LA FE   (Spain)

^b HOSPITAL INFANTIL LA FE   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA TOCOPHEROL; CHOLESTEROL; CHYLOMICRON; RETINOL; VITAMIN K GROUP;

ABDOMINAL DISTENSION; ARTICLE; CASE REPORT; CHOLESTEROL BLOOD LEVEL; DIET SUPPLEMENTATION; FEMALE; GIARDIA LAMBLIA; HUMAN; HYPOBETALIPOPROTEINEMIA; INTESTINE BIOPSY; MALE; PRESCHOOL CHILD; STEATORRHEA;

CELIAC DISEASE; CHILD; CHILD, PRESCHOOL; CHYLOMICRONS; DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; INFANT; LIPOPROTEINS; MALE;

EID: 12644312225     PISSN: 03024342     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (15)

1. Anderson C, Townley RRW, Freeman M, Johansen P. Unusual causes of steatorrhea in infancy and childhood. Med J Aust 1961; 11:617-622.
2. Buernstein M, Schelnik KR, Morfin R. Rapid method for the isolation of lipoproteins from human serum by precipitation with polianions. J Lipid Res 1970; 11:583-586.
3. Ishikawa TT, Brazier JB, Steiner PMS, Stewart LE, Gartside PS, Gluck CJ. A study of the heparin-manganese cloride method for determination of plasma lipoprotein cholesterol concentration. Lipids 1976; 11:628-633.
4. Sugiura M, Oikawa T, Hirano K, Maeda H, Yoshimura H, Karatsu T. A simple colorimetric method for determination of serum triglycerides glycerol with lipoprotein lipase and glycerol dehydrogenase. Clin Chem Acta 1977; 81:125-130.
5. Henck CC, Schlierf G. Nephelometry of apolipoprotein B in human serum. Clin Chem 1979; 25:221-226.
6. Granot E, Deckelbaum RJ. Hypocholesterolemia in childhood. J Pediatr 1989; 115.171-185.
7. Levy E, Chouraqui JP, Roy CC. Steatorrhea and disorders of chylomicron synthesis and secretion. Pediatr Clin North Am 1988; 35:53-67.
8. Roy CC, Levy E, Green PHR, Sniderman A, Letarte J, Buts JP y cols. Malabsortion, hypocolesterolemia, and fat-filled enterocytes with increased intestinal apoprotein B. Chylomicron retention disease. Gastroenterology 1987; 92:390-399.
9. Lacaille F, Bratos M, Bouma ME, Jos J, Schmitz J, Rey J. La maladie d'Anderson. Étude clinique et morphologique de 7 cas. Arch Fr Pediatr 1989; 46:491-498.
10. Hebert PN, Assman G, Gotto AM Jr, Fredrickson DS. Familial lipoprotein deficiency: abetalipoproteinemia, hypobetalipoproteinemia and Tangier disease. En: Stanbury JB, Wyngaarden JB, Fredrickson DS, Goldstein JL, Brown MS (eds). The metabolic bases of inherited disease. New York: McGraw Hill, 1982;589-621.
11. Takashima Y, Kodama T, Iida H, Kawamura M, Aburadani H, Itakura H y cols. Normotriglyceridemic betalipoproteinemia in infancy: An isolated apolipoprotein deficiency. Pediatrics 1985; 75:541-546.
12. Cottrill C, Glueck CJ, Leuba V, Millet F, Puppione D, Brown WV. Familial homozygous hypobetalipoproteinemia. Metabolism 1974; 23:779-791.
13. Bouma ME, Beucler I, Aggerbeck LP, Infante R, Schmitz J. J Clin Invest 1986; 78.398-410.
14. Pessah M, Benlian P, Beucler I, Loux N, Schmitz J, Junien C, Infante R. Anderson's disease: genetic exclusion of the apolipoprotein-B gene in two families. J Clin Invest 1991; 87:367-370.
15. Strich D, Goldstein R, Phillips A, Shemer R, Golberg Y, Razin A, Freier S. Anderson's disease: No linkage to the Apo B locus. J Pediatr Gatroenterol Nutr 1993; 16:257-264.