Peripheral blood lymphocyte appearance in a case of I cell disease

Journal of Clinical Pathology

Volumn 54, Issue 9, 2001, Pages 724-726

  Van der Meer, W ^a   Jakobs, B S ^a   Bocca, G ^a   Smeitink, J A M ^a   Schuurmans Steckhoven, J H ^a   De Keijzer, M H ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

I cell disease; Inclusion bodies; Lymphocytes

Indexed keywords

LIGAND; LYSOSOME ENZYME; MANNOSE 6 PHOSPHATE;

ARTICLE; BLOOD SMEAR; CASE REPORT; CELL INCLUSION; CELL STRUCTURE; CHILD; ENZYME ACTIVITY; FEMALE; FIBROBLAST; HUMAN; LYSOSOME; MACROMOLECULE; MUCOLIPIDOSIS TYPE 2; PERIODIC ACID SCHIFF STAIN; PERIPHERAL LYMPHOCYTE; PRIORITY JOURNAL;

EID: 0034839668     PISSN: 00219746     EISSN: None     Source Type: Journal    
DOI: 10.1136/jcp.54.9.724     Document Type: Article

References (10)

1. Mutant enzymatic and cytological phenotypes in cultured human fibroblasts
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3. I-cell disease: A case report and review of the literature
4. Histochemical and ultrastructural studies of inclusion bodies found in tissues from three siblings with I-cell disease
5. I-cell disease, a case report and review of the literature
6. Ultrastructural study of so-called curvilinear bodies and fingerprint structures in lymphocytes in late-infantile amaurotic idiocy
7. Diagnosdek van lysosomale stapelingsziekten
8. I-cell disease: A clinical picture
9. An autopsy case of I-cell disease