CONGENITAL DYSERYTHROPOIETIC ANEMIAS
\kənd͡ʒˈɛnɪtə͡l dˌa͡ɪsəɹˌɪθɹəpɔ͡ɪˈɛtɪk ɐnˈiːmi͡əz], \kəndʒˈɛnɪtəl dˌaɪsəɹˌɪθɹəpɔɪˈɛtɪk ɐnˈiːmiəz], \k_ə_n_dʒ_ˈɛ_n_ɪ_t_əl d_ˌaɪ_s_ə_ɹ_ˌɪ_θ_ɹ_ə_p_ɔɪ_ˈɛ_t_ɪ_k ɐ_n_ˈiː_m_iə_z]\
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A familial disorder characterized by anemia with multinuclear erythroblasts, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors. Type II is the most common of the 3 types of congenital dyserythropoietic anemia; it is often referred to as HEMPAS, based on the Hereditary Erythroblast Multinuclearity with Positive Acidified Serum test.
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Platidiam
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Nearby Words
- congenital defects
- congenital disease
- congenital disorder
- congenital disorders
- congenital dyserythropoietic anemia
- Congenital Dyserythropoietic Anemias
- congenital ectodermal defect
- congenital ectodermal defects
- congenital elephantiasis
- congenital erythropoietic porphyria
- congenital erythropoietic porphyrias