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Considering immunologic and genetic evaluation for HLH in neuroinflammation: A case of Griscelli syndrome type 2 with neurological symptoms and a lack of albinism.
Woodward, Kristine E; Shah, Ravi M; Benseler, Susanne; Wei, Xing-Chang; Ng, Denise; Grossman, Jennifer; Hahn, Christopher; Thomas, Mary Ann; Wright, Nicola A M; Appendino, Juan Pablo.
Affiliation
  • Woodward KE; Division of Clinical Neuroscience, Department of Pediatrics, Alberta Children's Hospital, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Shah RM; Division of Pediatric Oncology and BMT, Department of Pediatrics, Alberta Children's Hospital, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Benseler S; Division of Pediatric Rheumatology, Department of Pediatrics, Alberta Children's Hospital, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Wei XC; Department of Radiology, Alberta Children's Hospital, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Ng D; Division of Neuropathology, Department of Pathology and Laboratory Medicine, Foothills Medical Centre, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Grossman J; Department of Hematology, Foothills Medical Centre, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Hahn C; Division of Neurology, Department of Clinical Neurosciences, Foothills Medical Centre, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Thomas MA; Department of Medical Genetics, Alberta Children's Hospital, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Wright NAM; Division of Pediatric Hematology and Immunology, Department of Pediatrics, Alberta Children's Hospital, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Appendino JP; Division of Clinical Neuroscience, Department of Pediatrics, Alberta Children's Hospital, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Pediatr Blood Cancer ; 67(8): e28312, 2020 08.
Article de En | MEDLINE | ID: mdl-32459386

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Piébaldisme / Lymphohistiocytose hémophagocytaire / Protéines rab27 liant le GTP / Maladies d'immunodéficience primaire Type d'étude: Diagnostic_studies Limites: Adolescent / Humans / Male Langue: En Journal: Pediatr Blood Cancer Sujet du journal: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Année: 2020 Type de document: Article Pays d'affiliation: Canada

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Piébaldisme / Lymphohistiocytose hémophagocytaire / Protéines rab27 liant le GTP / Maladies d'immunodéficience primaire Type d'étude: Diagnostic_studies Limites: Adolescent / Humans / Male Langue: En Journal: Pediatr Blood Cancer Sujet du journal: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Année: 2020 Type de document: Article Pays d'affiliation: Canada