The association between juvenile xanthogranulomas in neurofibromatosis type 1 patients and the development of leukaemia: A systematic review

Author:

Meyer S. N.1ORCID,Vaughn A.1,Li Y.2ORCID,Studer A. C.3ORCID,Rauen K. A.4,Kiuru M.15ORCID

Affiliation:

1. Department of Dermatology University of California, Davis School of Medicine Sacramento California USA

2. Department of Public Health Sciences University of California, School of Medicine Sacramento California USA

3. Blaisdell Medical Library University of California, Davis Sacramento California USA

4. Department of Pediatrics University of California, Davis School of Medicine Sacramento California USA

5. Department of Pathology and Laboratory Medicine University of California, Davis School of Medicine Sacramento California USA

Funder

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Publisher

Wiley

Subject

Infectious Diseases,Dermatology

Reference8 articles.

1. Mitotic recombination and compound-heterozygous mutations are predominant NF1-inactivating mechanisms in children with juvenile myelomonocytic leukemia and neurofibromatosis type 1

2. Chronic myelomonocytic leukemia in childhood: a retrospective analysis of 110 cases. European Working Group on Myelodysplastic Syndromes in Childhood (EWOG‐MDS);Niemeyer CM;Blood,1997

3. How I treat juvenile myelomonocytic leukemia

4. Juvenile myelomonocytic leukemia‐a comprehensive review and recent advances in management;Gupta AK;Am J Blood Res,2021

5. Juvenile Xanthogranuloma, Neurofibromatosis, and Juvenile Chronic Myelogenous Leukemia

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