Congenital Dyserythropoietic Anemia
What's New
Last Posted: Mar 29, 2023
- Evaluation of the main regulators of systemic iron homeostasis in pyruvate kinase deficiency.
Zaninoni Anna, et al. Scientific reports 2023 0 (1) 4395 - [Using target next-generation sequencing assay in diagnosing of 46 patients with suspected congenital anemias].
Li Y, et al. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2018 0 (5) 414-419 - Clinical and genetic features of congenital dyserythropoietic anemia (CDA).
Moreno-Carralero María-Isabel, et al. European journal of haematology 2018 0 (3) 368-378 - Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias.
Russo Roberta, et al. American journal of hematology 2018 0 (5) 672-682 - Compound heterozygosity for two novel mutations of the SEC23B gene in congenital dyserythropoietic anemia type II.
Chen Shanshan, et al. International journal of hematology 2021 0 (3) 390-394 - Congenital dyserythropoietic anemia and drug-induced liver injury present as bland cholestasis: A case report.
Han Yue, et al. Experimental and therapeutic medicine 2021 0 (5) 456 - Local Coverage Determination (LCD): Flow Cytometry (L33661)
The U.S. Centers for Medicare & Medicaid Services - Congenital dyserythropoietic anemia
From NCATS Genetic and Rare Diseases Information Center - Congenital dyserythropoietic anemia type 1
From NCATS Genetic and Rare Diseases Information Center - Congenital dyserythropoietic anemia type 2
From NCATS Genetic and Rare Diseases Information Center
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Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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