Pearson's marrow/pancreas syndrome: haematological features associated with deletion and duplication of mitochondrial DNA

التفاصيل البيبلوغرافية
العنوان: Pearson's marrow/pancreas syndrome: haematological features associated with deletion and duplication of mitochondrial DNA
المؤلفون: M. Brockington, C. E. Woodward, Owen Smith, Ian Hann
المصدر: British journal of haematology. 90(2)
سنة النشر: 1995
مصطلحات موضوعية: medicine.medical_specialty, Mitochondrial DNA, Pancreatic disease, Biology, Neutropenia, DNA, Mitochondrial, Sideroblastic anemia, Internal medicine, medicine, Humans, Bone Marrow Diseases, Pearson syndrome, Infant, Pancreatic Diseases, Hematology, Gene rearrangement, Syndrome, medicine.disease, Anemia, Sideroblastic, Blotting, Southern, Endocrinology, medicine.anatomical_structure, Multigene Family, Female, Bone marrow, Pancreas, Gene Deletion
الوصف: Summary. Pearson's marrow/pancreas syndrome (PS) is a rare, often fatal, disorder of infancy that is characterized by impaired bone marrow, exocrine pancreatic, hepatic and renal function. Large-scale rearrangements of mitochondrial DNA (mtDNA) are present in blood. We report a patient with PS who has predominantly impaired haemopoiesis manifesting as sideroblastic anaemia, vacuolization of bone marrow precursors, and neutropenia. 77% of bone marrow mtDNA was rearranged (64% deleted an 13% duplicated). We suggest that rearrangements of mtDNA should be sought in all infants presenting with sideroblastic anaemia.
تدمد: 0007-1048
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4720b6adc464027a7d2f66c60d2ca01f
https://pubmed.ncbi.nlm.nih.gov/7794775
Rights: CLOSED
رقم الانضمام: edsair.doi.dedup.....4720b6adc464027a7d2f66c60d2ca01f
قاعدة البيانات: OpenAIRE