Pearson syndrome

Am J Hematol. 2023 Mar;98(3):527-528. doi: 10.1002/ajh.26794. Epub 2022 Dec 5.

Authors

Aditya Tedjaseputra¹, Kottayam Radhakrishnan^{1

2}, Michelle Martin², Peter Downie², Melina Stergiotis², Barbara J Bain³

Affiliations

¹ Monash Haematology, Monash Health, Melbourne, Australia.
² Paediatric Haematology Oncology, Children's Cancer Centre, Monash Children's Hospital, Monash Health, Melbourne, Australia.
³ Centre for Haematology, St Mary's Hospital Campus of Imperial College Faculty of Medicine, St Mary's Hospital, London, UK.

PMID: 36436195
DOI: 10.1002/ajh.26794

No abstract available

Publication types

Case Reports

MeSH terms

Congenital Bone Marrow Failure Syndromes
DNA, Mitochondrial
Humans
Lipid Metabolism, Inborn Errors*
Mitochondrial Diseases*
Muscular Diseases*

Substances

DNA, Mitochondrial

Supplementary concepts

VLCAD deficiency