Bone marrow features in Pearson syndrome with neonatal onset: A case report and review of the literature

Author:

Tadiotto Elisa1ORCID,Maines Evelina2,Degani Daniela1,Balter Rita3,Bordugo Andrea4,Cesaro Simone3ORCID

Affiliation:

1. Pediatric Clinic; Department of Life and Reproduction Sciences; Azienda Ospedaliera Universitaria Integrata; Verona Italy

2. Pediatric Unit; Provincial Centre for Rare Diseases; Department of Maternal and Child Health; Azienda Provinciale per i Servizi Sanitari; Trento Italy

3. Pediatric Hematology and Oncology Unit; Department of Pediatrics; Azienda Ospedaliera Universitaria Integrata; Verona Italy

4. Department of Pediatrics; Regional Centre for Newborn Screening; Diagnosis and Treatment of Inherited Metabolic Diseases and Congenital Endocrine Diseases; Azienda Ospedaliera Universitaria Integrata; Verona Italy

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Reference20 articles.

1. A new syndrome of refractory sideroblastic anemia with vacuolization of bone marrow precursors and exocrine pancreatic dysfunction;Pearson;J Pediatr.,1979

2. Pearson syndrome: a retrospective cohort study from the Marrow Failure Study Group of A.I.E.O.P. (Associazione Italiana Emato-Oncologia Pediatrica);Farruggia;JIMD Rep.,2016

3. Pearson syndrome in the neonatal period. Two case reports and review of the literature;Manea;J Pediatr Hematol Oncol,2009

4. A novel mitochondrial DNA deletion in a patient with Pearson syndrome and neonatal diabetes mellitus provides insight into disease etiology, severity and progression;Chen;Mitochondrial DNA A DNA Mapp Seq Anal,2016

5. Invasive aspergillosis in two patients with Pearson syndrome;Warris;Pediatr Infect Dis J,1999

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