Clinical and genetic features of four patients with Pearson syndrome-Reference-Cited by-同舟云学术

Clinical and genetic features of four patients with Pearson syndrome

Published:2022-02-04 Issue:5 Volume:101 Page:e28793
ISSN:0025-7974
Container-title:Medicine
language:en
Short-container-title:

Author:

Son Ji Soo,Seo Go Hun,Kim Yoon-Myung,Kim Gu-Hwan,Jin Hee Kyung,Bae Jae-sung,Im Ho Joon,Yoo Han-Wook,Lee Beom Hee

Funder

National Research Foundation of Korea

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference22 articles.

1. Allogeneic bone marrow transplantation for Pearson's syndrome;Faraci;Bone Marrow Transplant,2007

2. Paediatric single mitochondrial DNA deletion disorders: an overlapping spectrum of disease;Broomfield;J Inherit Metab Dis,2015

3. Pearson Syndrome: A Retrospective Cohort Study from the Marrow Failure Study Group of A.I.E;Farruggia;O P (Associazione Italiana Emato-Oncologia Pediatrica) JIMD Rep,2016

4. The epidemiology of mitochondrial disorders--past, present and future;Schaefer;Biochim Biophys Acta,2004

5. Clinical and laboratory findings in referrals for mitochondrial DNA analysis;Lamont;Arch Dis Child,1998

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1. Clinical and biochemical footprints of inherited metabolic disease. XVI. Hematological abnormalities;Molecular Genetics and Metabolism;2023-12

2. Successful cord blood transplantation for del7q myelodysplastic syndrome in Pearson marrow pancreas syndrome;American Journal of Hematology;2023-09-21

3. Hemolytic Anemia Requiring Splenectomy in Leigh-Like Syndrome due to the Variant m.10191T>C in MT-ND3;Journal of Hematology;2023-08

4. A Case Report on Pearson Syndrome With Emphasis on Genetic Screening in Patients Presenting With Sideroblastic Anemia and Lactic Acidosis;Cureus;2023-01-19

5. Adrenal Dysfunction in Mitochondrial Diseases;International Journal of Molecular Sciences;2023-01-06