Pearson Syndrome

Pearson syndrome is a rare disease that affects the bone marrow and pancreas. It is caused by a mutation in the mitochondrial DNA. Symptoms include pancreatic insufficiency, anemia, neutropenia, and thrombocytopenia which can lead to feeling weak, tired, and bruising more easily. Here is the latest research on Pearson Syndrome.

April 11, 2021
Open Access

Haematological characteristics and spontaneous haematological recovery in Pearson syndrome.

British Journal of Haematology
Ayami YoshimiCharlotte M Niemeyer
February 27, 2021
Case Report
Open Access

Identification of a novel large deletion of the mitochondrial DNA in an infant with Pearson syndrome: a case report.

Translational Pediatrics
Rui LiuYuan-Zong Song
February 16, 2021

A useful method to diagnose Pearson syndrome mimicking Diamond-Blackfan anemia.

Pediatrics International : Official Journal of the Japan Pediatric Society
Toyoki NishimuraHiroshi Moritake
November 18, 2020
Case Report

Acquisition of monosomy 7 and a RUNX1 mutation in Pearson syndrome.

Pediatric Blood & Cancer
Akira NishimuraAtsushi Manabe
October 28, 2020
Open Access

The Phenotypic Spectrum of 47 Czech Patients with Single, Large-Scale Mitochondrial DNA Deletions

Brain Sciences
Nicole AnteneováTomas Honzik
August 9, 2020
Comment / Editorial

Pearson Syndrome: Spontaneously Recovering Anemia and Hypoparathyroidism - Correspondence.

Indian Journal of Pediatrics
Josef FinstererShubha R Phadke
June 17, 2020
Case Report

Pearson Syndrome: Spontaneously Recovering Anemia and Hypoparathyroidism.

Indian Journal of Pediatrics
Mayank Nilay, Shubha R Phadke
March 22, 2020
Open Access

Propionic acidemia: an extremely rare cause of hemophagocytic lymphohistiocytosis in an infant

Archivos argentinos de pediatría
Sultan Aydin KökerEsra Şevketoğlu
January 24, 2020
Case Report
Open Access

Pearson syndrome: a rare inborn error of metabolism with bone marrow morphology providing a clue to diagnosis

Sudanese Journal of Paediatrics
Jyothi Muni ReddyShanthala Devi
January 12, 2020
Review
Open Access

Mitochondrial DNA mutations in renal disease: an overview.

Pediatric Nephrology : Journal of the International Pediatric Nephrology Association
Larissa P GoversDetlef Bockenhauer
December 18, 2019
Review
Open Access

Pediatric liver diseases and ocular changes: What hepatologists and ophthalmologists should know and share with each other

Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver
Livio VitielloPietro Vajro
December 12, 2019
Open Access

Broadening the phenotypic spectrum of Pearson syndrome: Five new cases and a review of the literature

American Journal of Medical Genetics. Part a
K Taylor WildRebecca D Ganetzky
October 18, 2019
Case Report

Delayed Onset of Retinopathy of Prematurity Associated With Mitochondrial Dysfunction and Pearson Syndrome

Journal of Pediatric Ophthalmology and Strabismus
Nimesh A PatelAudina M Berrocal
September 3, 2019
Case Report
Open Access

Pearson marrow-pancreas syndrome with cardiac conduction abnormality necessitating prophylactic pacemaker implantation.

Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc
Mats Steffi Jennifer, Daniel Cortez
August 27, 2019
Review

Mitochondrial DNA deletion syndrome: a case report and literature review

Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery
Y H ZhuQ J Wang

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