Histologic features of the liver in type Ia glycogen storage disease: Comparative study between different age groups and consecutive biopsies

Pediatric and Developmental Pathology

Volumn 5, Issue 3, 2002, Pages 299-304

  Göǧüş, Safye ^a   Koçak, Nurten ^a   Clv, Gönenç ^a   Karabulut, Erdem ^a   Akçören, Zuhal ^a   Kale, Gülsev ^a   Çaǧlar, Melda ^a  

^a HACETTEPE UNIVERSITY   (Turkey)

Author keywords

Glycogen storage disease type Ia; Liver biopsy; Liver fibrosis

Indexed keywords

AGE DISTRIBUTION; ARTICLE; CHILD; CLINICAL ARTICLE; COMPARATIVE STUDY; FATTY LIVER; GLYCOGEN STORAGE DISEASE TYPE 1; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; LIVER BIOPSY; LIVER FIBROSIS; PRIORITY JOURNAL; STATISTICAL ANALYSIS;

ADOLESCENT; AGE DISTRIBUTION; BIOPSY; CHILD; CHILD, PRESCHOOL; FATTY LIVER; GLUCOSE-6-PHOSPHATASE; GLYCOGEN STORAGE DISEASE TYPE I; HUMANS; INFANT; INFANT, NEWBORN; LIVER; LIVER CIRRHOSIS;

EID: 0036293277     PISSN: 10935266     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10024-001-0139-6     Document Type: Article

References (9)

1. Glycogen storage disease, types I to X. Criteria for morphologic diagnosis
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3. Glycogen storage diseases
4. Liver diseases in infancy
5. Histopathologic approach to metabolic liver disease: Part 1
6. Severe liver fibrosis in argininosuccinic aciduria
7. Mallory bodies in a patient with type Ia glycogen storage disease
8. Reliability of histological criteria in glycogen storage disease of the liver
9. Hepatic fibrosis in the mucopolysaccharidoses