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[A regenerative anemia in infants: 2 cases of Pearson´s syndrome].

作者信息

Martínez de Zabarte Fernández José M, Rodríguez-Vigil Iturrate Carmen, Martínez Faci Cristina, García Jiménez Inmaculada, Murillo Sanjuan Laura, Muñoz Mellado Ascensión

机构信息

Servicio de Pediatría, Hospital Universitario Miguel Servet, Zaragoza, España.

Unidad de Oncohematología Pediátrica, Servicio de Pediatría, Hospital Universitario Miguel Servet, Zaragoza, España.

出版信息

Arch Argent Pediatr. 2017 Feb 1;115(1):e24-e27. doi: 10.5546/aap.2017.e24.

Abstract

Anemia is very common in infants. Although its causes are usually not severe and treatable, proper etiologic diagnosis should be established. When anemia is non-regenerative, it can be caused by aplastic anemia, myelodysplastic syndrome, bone marrow infiltration or hematopoietic factors deficiencies. Another possible cause is Pearson's syndrome, a rare mitochondrial disease that causes non-regenerative anemia associated with other cytopenias, pancreatic insufficiency, lactic acidosis and great variability in clinical presentation conditioned by heteroplasmy. It is characteristic to find in bone marrow studies variable vacuolization in erythroblastic progenitors and ring sideroblasts. The diagnosis is established by genetic study of mitochondrial deoxyribonucleic acid performed by Southern blot analysis (complete mitochondrial deoxyribonucleic acid amplification by polymerase chain reaction -long), obtaining 70-80% deletion of 4977 bp (NMD 8343-13459). There is no curative therapy and support treatment is the only available nowadays. Death is frequent in early years of life.

摘要

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