Systemic progression of type IV glycogen storage disease after liver transplantation

Journal of Pediatric Gastroenterology and Nutrition

Volumn 51, Issue 5, 2010, Pages 661-664

  Willot, Stephanie ^a   Marchand, Valerie ^a   Rasquin, Andree ^a   Alvarez, Fernando ^a   Martin, Steven R ^a  

^a UNIVERSITY OF MONTREAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ALKALINE PHOSPHATASE; AMYLOPECTIN; ANTIBIOTIC AGENT; AZATHIOPRINE; BILIRUBIN; CAPTOPRIL; CYCLOSPORIN; DIGOXIN; DIURETIC AGENT; GAMMA GLUTAMYLTRANSFERASE; GANCICLOVIR; LYMPHOCYTE ANTIBODY; MYCOPHENOLIC ACID 2 MORPHOLINOETHYL ESTER; PAMIDRONIC ACID; PREDNISONE; STEROID; TACROLIMUS;

ACUTE KIDNEY TUBULE NECROSIS; ALKALINE PHOSPHATASE BLOOD LEVEL; ANTIBIOTIC THERAPY; ARTICLE; ATELECTASIS; AUTOPSY; BILE DUCT DILATATION; BILIRUBIN BLOOD LEVEL; CARDIOMYOPATHY; CASE REPORT; CAUSE OF DEATH; CELL INFILTRATION; CHOLANGIOGRAPHY; CHOLEDOCHOJEJUNOSTOMY; CYTOMEGALOVIRUS INFECTION; CYTOPLASM; DEVELOPMENTAL DISORDER; DISEASE COURSE; DISEASE SEVERITY; DIURETIC THERAPY; DOPPLER ECHOGRAPHY; ECHOCARDIOGRAPHY; ELECTRON MICROSCOPY; FEVER; GAMMA GLUTAMYL TRANSFERASE BLOOD LEVEL; GLYCOGEN STORAGE DISEASE TYPE 4; HEART FAILURE; HEART HYPERTROPHY; HEART LEFT VENTRICLE HYPERTROPHY; HEART MUSCLE BIOPSY; HEART MUSCLE CELL; HEART MUSCLE CONTRACTILITY; HEART MUSCLE FIBROSIS; HEPATICOGASTROSTOMY; HEPATOMEGALY; HEPATOSPLENOMEGALY; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNOSUPPRESSIVE TREATMENT; INFANT; INTRAHEPATIC BILE DUCT; LIVER BIOPSY; LIVER CIRRHOSIS; LIVER DYSFUNCTION; LIVER FAILURE; LIVER GRAFT REJECTION; LIVER INJURY; LIVER TRANSPLANTATION; LUNG BIOPSY; LUNG EDEMA; LUNG INFILTRATE; LUNG INSUFFICIENCY; MALE; MASTOIDECTOMY; MOUTH EDEMA; MUSCLE HYPOTONIA; MYCOPLASMOSIS; NECK PAIN; NEUROLOGIC EXAMINATION; OSTEOMYELITIS; OSTEOPENIA; OTORRHEA; PERICARDIAL EFFUSION; PERIODIC ACID SCHIFF STAIN; PERIPHERAL EDEMA; PLEURA EFFUSION; PNEUMONIA; PNEUMOTHORAX; POLYSEROSITIS; PORTAL HYPERTENSION; PRIORITY JOURNAL; RESPIRATORY DISTRESS SYNDROME; SCLEROSING CHOLANGITIS; SKIN EDEMA; SPLENOMEGALY; STOMACH SURGERY; SYNOVITIS; THORAX RADIOGRAPHY;

DISEASE PROGRESSION; FATAL OUTCOME; GLYCOGEN STORAGE DISEASE TYPE IV; HEART FAILURE; HUMANS; INFANT; LIVER TRANSPLANTATION; MALE; POSTOPERATIVE COMPLICATIONS;

EID: 78149281391     PISSN: 02772116     EISSN: None     Source Type: Journal    
DOI: 10.1097/MPG.0b013e3181d29780     Document Type: Article

References (12)

1. Davis MK, Weinstein DA. Liver transplantation in children with glycogen storage disease: controversies and evaluation of the risk/benefit of this procedure. Pediatr Transplant 2008;12:137-45.
2. Matern D, Starzl TE, Arnaout W, et al. Liver transplantation for glycogen storage disease types I, III, and IV. Eur J Pediatr 1999;158:S43-8.
3. Starzl TE, Demetris AJ, Trucco M, et al. Chimerism after liver transplantation for type IV glycogen storage disease and type 1 Gaucher's disease. N Engl J Med 1993;18:745-9.
4. Rosenthal P, Podesta L, Grier R, et al. Failure of liver transplantation to diminish cardiac deposits of amylopectin and leukocyte inclusions in type IV glycogen storage disease. Liver Transpl Surg 1995;1:373-6.
5. Sokal EM, Van Hoof F, Alberti D, et al. Progressive cardiac failure following orthotopic liver transplantation for type IV glycogenosis. Eur J Pediatr 1992;151:200-3.
6. Selby R, Starzl TE, Yunis E, et al. Liver transplantation for type IV glycogen storage disease. N Engl J Med 1991;324:39-42.
7. Munns CF, Rauch F, Mier RJ, et al. Respiratory distress with pami-dronate treatment in infants with severe osteogenesis imperfecta. Bone 2004;35:231-4.
8. Pietschmann P, Stohlawetz P, Brosch S, et al. The effect of alendronate on cytokine production, adhesion molecule expression, and transen-dothelial migration of human peripheral blood mononuclear cells. Calcif Tissue Int 1998;63:325-30.
9. Endo Y, Nakamura M, Kikuchi T, et al. Aminoalkylbisphosphonates, potent inhibitors of bone resorption, induce a prolonged stimulation of histamine synthesis and increase macrophages, granulocytes, and os-teoclasts in vivo. Calcif Tissue Int 1993;52:248-54.
10. Bruno C, van Diggelen OP, Cassandrini D, et al. Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV). Neurology 2004;63:1053-8.
11. Moses SW, Parvari R. The variable presentations of glycogen storage disease type IV: a review of clinical, enzymatic and molecular studies. Curr Mol Med 2002;2:177-88.
12. Bao Y, Kishnani P, Wu JY, et al. Hepatic and neuromuscular forms of glycogen storage disease type IV caused by mutations in the same glycogen-branching enzyme gene. J Clin Invest 1996;97:941-8.