Congenital Atypical Microcytic Anemia Accompanied by Iron Deficiency and Accumulation
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Keywords
atypical iron deficiency anemia,, aceruloplasminemia, copper deficiency, ferritin elevation
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References
Marchi G, Busti F, Lira Zidanes A, Castagna A, Girelli D. Aceruloplasminemia: A severe neurodegenerative disorder deserving an early diagnosis. Front Neurosci 2019;13:325.https://doi.org/10.3389/fnins.2019.00325PMid:31024241 PMCid:PMC64605672.
Miyajima H. Aceruloplasminemia. Neuropathology 2015;35:83-90.https://doi.org/10.1111/neup.12149PMid:251684553.
Migone De Amicis M., Rimondi A.,Elli L., Motta I.Acquired refractory iron deficiency anemia.Mediterr J Hematol Infect Dis 2021, 13(1): e2021028https://doi.org/10.4084/MJHID.2021.028PMid:34007416 PMCid:PMC81148944.
Vila Cuenca M, Marchi G, Barqué A, Esteban-Jurado C, Marchetto A, Giorgetti A, Chelban V, Houlden H, Wood NW, Piubelli C, Dorigatti Borges M, Martins de Albuquerque D, Yotsumoto Fertrin K, Jové-Buxeda E, Sanchez-Delgado J, Baena-Díez N, Burnyte B, Utkus A, Busti F, Kaubrys G, Suku E, Kowalczyk K, Karaszewski B, Porter JB, Pollard S, Eleftheriou P, Bignell P, Girelli D, Sanchez M. Genetic and clinical heterogeneity in thirteen new cases with aceruloplasminemia. Atypical anemia as a clue for an early diagnosis. Int J Mol Sci 2020;21:2374.https://doi.org/10.3390/ijms21072374PMid:32235485 PMCid:PMC71780745.
Miyajima H, Hosoi Y. Aceruloplasminemia. Gene reviews [internet]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, et al., eds. 1993. Seattle, WA: University of Washington. 2018.6.
Lanzkowsky P. Classification and diagnosis of anemia in children. In: Lanzkowsky P, Lipton JM, Fish JD, eds. Lanzkowsky's manual of pediatric Hematology and oncology. 6thed. India: MPS Limited. 2016; 32-41.https://doi.org/10.1016/B978-0-12-801368-7.00003-X7.
Goodnough LT, Nemeth E. Iron deficiency and related disorders. In: Greer JP, Arber DA, Glader B, List AF, Means Jr RT, Paraskevas F, Rodges GM, eds. Wintrobe's clinical Hematology. 13thed. Philadelphia: Lippincott Williams & Wilkins. 2014; 1419-798.
Vroegindeweij LHP, Langendonk JG, Langeveld M, Hoogendoorn M, Kievit AJA, Di Raimondo D, Wilson JHP, Boon AJW. New insights in the neurological phenotype of aceruloplasminemia in Caucasian patients. Parkinsonism Relat Disord 2017;36:33-40.https://doi.org/10.1016/j.parkreldis.2016.12.010PMid:280129539.ùKato T, Daimon M, Kawanami T, Ikezawa Y, Sasaki
H, Maeda K. Islet changes in hereditary ceruloplasmin deficiency. Hum Pathol 1997;28:499-502.https://doi.org/10.1016/S0046-8177(97)90041-110.
Fleming MD. Disorders of iron and copper metabolism, the sideroblastic anemias, and lead toxicity. In: Orkin SH, FisherDE, Ginsberg D, Look AT, Lux SE, Nathan DG, eds. Nathan and Oski's Hematology and Oncology Infancy and Childhood. 8thed. Philadelphia: Elsevier Saunders. 2015; 344-81.
Miyajima H. Aceruloplasminemia. Neuropathology 2015;35:83-90.https://doi.org/10.1111/neup.12149PMid:251684553.
Migone De Amicis M., Rimondi A.,Elli L., Motta I.Acquired refractory iron deficiency anemia.Mediterr J Hematol Infect Dis 2021, 13(1): e2021028https://doi.org/10.4084/MJHID.2021.028PMid:34007416 PMCid:PMC81148944.
Vila Cuenca M, Marchi G, Barqué A, Esteban-Jurado C, Marchetto A, Giorgetti A, Chelban V, Houlden H, Wood NW, Piubelli C, Dorigatti Borges M, Martins de Albuquerque D, Yotsumoto Fertrin K, Jové-Buxeda E, Sanchez-Delgado J, Baena-Díez N, Burnyte B, Utkus A, Busti F, Kaubrys G, Suku E, Kowalczyk K, Karaszewski B, Porter JB, Pollard S, Eleftheriou P, Bignell P, Girelli D, Sanchez M. Genetic and clinical heterogeneity in thirteen new cases with aceruloplasminemia. Atypical anemia as a clue for an early diagnosis. Int J Mol Sci 2020;21:2374.https://doi.org/10.3390/ijms21072374PMid:32235485 PMCid:PMC71780745.
Miyajima H, Hosoi Y. Aceruloplasminemia. Gene reviews [internet]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, et al., eds. 1993. Seattle, WA: University of Washington. 2018.6.
Lanzkowsky P. Classification and diagnosis of anemia in children. In: Lanzkowsky P, Lipton JM, Fish JD, eds. Lanzkowsky's manual of pediatric Hematology and oncology. 6thed. India: MPS Limited. 2016; 32-41.https://doi.org/10.1016/B978-0-12-801368-7.00003-X7.
Goodnough LT, Nemeth E. Iron deficiency and related disorders. In: Greer JP, Arber DA, Glader B, List AF, Means Jr RT, Paraskevas F, Rodges GM, eds. Wintrobe's clinical Hematology. 13thed. Philadelphia: Lippincott Williams & Wilkins. 2014; 1419-798.
Vroegindeweij LHP, Langendonk JG, Langeveld M, Hoogendoorn M, Kievit AJA, Di Raimondo D, Wilson JHP, Boon AJW. New insights in the neurological phenotype of aceruloplasminemia in Caucasian patients. Parkinsonism Relat Disord 2017;36:33-40.https://doi.org/10.1016/j.parkreldis.2016.12.010PMid:280129539.ùKato T, Daimon M, Kawanami T, Ikezawa Y, Sasaki
H, Maeda K. Islet changes in hereditary ceruloplasmin deficiency. Hum Pathol 1997;28:499-502.https://doi.org/10.1016/S0046-8177(97)90041-110.
Fleming MD. Disorders of iron and copper metabolism, the sideroblastic anemias, and lead toxicity. In: Orkin SH, FisherDE, Ginsberg D, Look AT, Lux SE, Nathan DG, eds. Nathan and Oski's Hematology and Oncology Infancy and Childhood. 8thed. Philadelphia: Elsevier Saunders. 2015; 344-81.