Severe lactic acidosis and nephrolithiasis in an infant - Etiology?: Answer

Pediatric Nephrology

Volumn 21, Issue 6, 2006, Pages 763-765

  Güven, Ayfer Gür ^a   Koyun, Mustafa ^a   Artan, Reha ^a   Dursun, Oǧuz ^a   Baysal, Yunus Emre ^a   Akman, Sema ^a  

^a AKDENIZ UNIVERSITY   (Turkey)

Author keywords

Acidosis; Glycogen storage disease; Nephrolithiasis

Indexed keywords

BICARBONATE; CALCIUM; CHOLESTEROL; CITRATE POTASSIUM; CITRIC ACID; CREATININE; GLUCOSE 6 PHOSPHATASE; LACTIC ACID; LOW DENSITY LIPOPROTEIN; TRIACYLGLYCEROL; UBIQUINONE; URIC ACID; VERY LOW DENSITY LIPOPROTEIN; VITAMIN B COMPLEX; CALCIUM OXALATE; ALANINE AMINOTRANSFERASE; ALBUMIN; AMMONIA; ASPARTATE AMINOTRANSFERASE; BILIRUBIN; CHLORIDE; GLUCOSE; HEMOGLOBIN; HIGH DENSITY LIPOPROTEIN; NITROGEN; PHOSPHORUS; POTASSIUM; SODIUM; UREA;

ANION GAP; ARTICLE; ARTIFICIAL VENTILATION; CALCIUM OXALATE STONE; CALCIUM URINE LEVEL; CASE REPORT; CHOLESTEROL BLOOD LEVEL; CORPUS CALLOSUM AGENESIS; CREATININE URINE LEVEL; DISEASE SEVERITY; FEMALE; FLUID THERAPY; GLOMERULUS FILTRATION RATE; GLYCOGEN STORAGE DISEASE TYPE 1; HEMODIALYSIS; HEPATOMEGALY; HOSPITAL DISCHARGE; HUMAN; HUMAN TISSUE; HYPERCALCIURIA; HYPOGLYCEMIA; INFANT; INTENSIVE CARE; KIDNEY CALCIFICATION; KIDNEY TUBULE ACIDOSIS; LACTATE BLOOD LEVEL; LACTIC ACIDOSIS; LIVER BIOPSY; NEPHROLITHIASIS; PRIORITY JOURNAL; TRIACYLGLYCEROL BLOOD LEVEL; URIC ACID BLOOD LEVEL; URINE PH; UROLITHIASIS; BLOOD CHEMISTRY; BREATHING; BREATHING RATE; CLINICAL ARTICLE; CONSANGUINITY; DYSPNEA; ECHOGRAPHY; FOLLOW UP; GASTROENTERITIS; HEPATOSPLENOMEGALY; HUMAN CELL; INFRARED SPECTROSCOPY; KUSSMAUL BREATHING; LABORATORY TEST; METABOLIC ACIDOSIS; NOTE; RESTLESSNESS; TACHYCARDIA; TACHYPNEA; URINARY TRACT INFECTION; ALANINE AMINOTRANSFERASE BLOOD LEVEL; ASPARTATE AMINOTRANSFERASE BLOOD LEVEL; BLOOD PH; BREAST FEEDING; CARBON DIOXIDE TENSION; CREATININE BLOOD LEVEL; EMERGENCY HEALTH SERVICE; GLUCOSE BLOOD LEVEL; HOSPITAL ADMISSION; LEUKOCYTE COUNT; LYMPHOCYTE COUNT; THROMBOCYTE COUNT; UREA NITROGEN BLOOD LEVEL;

ACIDOSIS, LACTIC; FEMALE; GLYCOGEN STORAGE DISEASE TYPE I; HUMANS; INFANT; KIDNEY CALCULI; LIVER;

EID: 33646671879     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00467-006-0078-6     Document Type: Article

References (11)

1. Chen Y (2004) Glycogen storage diseases. In: Behrman RE, Kliegman RM, Jenson HB (eds) Textbook of pediatrics, 17th edn. WB Saunders, Philidelphia, PA, pp 469-475
2. Greenbaum LA (2004) Pathophysiology of body fluids and fluid therapy. In: Behrman RE, Kliegman RM, Jenson HB (eds) Textbook of pediatrics, 17th edn. WB Saunders, Philidelphia, PA, pp 191-252
3. Horslen S (2004) Genetic and metabolic disorders. I. Carbohydrate metabolism. In: Walker WA, Goulet O, Kleinman RE, Sherman PM, Shneider BL, Sanderson IR (eds) Pediatric gastrointestinal disease, volume II, 4th edn. Marcel Decker, New York, pp 1257-1274
4. Restaino I, Kaplan BS, Stanley C, Baker L (1993) Nephrolithiasis, hypocitraturia and a distal renal tubular acidification defect in type 1 glycogen storage disease. J Pediatr 122:392-396
5. Hulton SA (2001) Evaluation of urinary tract calculi in children. Arch Dis Child 84:320-323
6. Chen Y (2004) Defects in galactose metabolism. In: Behrman RE, Kliegman RM, Jenson HB (eds) Textbook of pediatrics, 17th edn. WB Saunders, Philidelphia, PA, pp 476-480
7. Ames RP (1986) The effects of antihypertensive drugs on serum lipids and lipoproteins, I. Diuretics. Drugs 32:260-278
8. Simöes A, Domingos F, Fortes A, Prata MM (2001) Type 1 glycogen storage disease and recurrent calcium nephrolithiasis. Nephrol Dial Transplant 16:1277-1279
9. Reitsma-Bierens WC (1993) Renal complications in glycogen storage disease type 1. Eur J Pediatr 152(Suppl 1):S60-S62
10. Chen YT, Coleman RA, Scheinman JI, Kolbeck PC, Sidbury JB (1988) Renal disease in type 1 glycogen storage disease. New Engl J Med 318:7-11
11. Chen YT (1991) Type 1 glycogen storage disease: Kidney involvement, pathogenesis and its treatment. Pediatr Nephrol 5:71-76