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 (ERYTHROID PRECURSOR CELLS). Type II is the most common of the 3 types; it is often referred to as HEMPAS, based on the Hereditary Erythroblast Multinuclearity with Positive Acidified Serum test.
推出的年份: 1991(1980)
副标题
树号: C15.378.071.141.150.095, C16.320.070.095
MeSH 单一 ID: D000742
进入的组:
Congenital Dyserythropoietic Anemia
Dyserythropoietic Anemia, Congenital
Anemia, Congenital Dyserythropoietic
Anemias, Congenital Dyserythropoietic
Congenital Dyserythropoietic Anemias
Dyserythropoietic Anemias, Congenital
Anemia, Dyserythropoietic, Congenital, Type II
Anemia, Dyserythropoietic, Congenital Type 2
Congenital Dyserythropoietic Anemia Type II
Dyserythropoietic Anemia, Congenital Type 2
Dyserythropoietic Anemia, Congenital, Type II
HEMPAS
HEMPAS Anemia
HEMPAS Anemias
Hereditary Erythroblast Multinuclearity with Positive Acidified Serum
Hereditary Erythroblastic Multinuclearity with Positive Acidified-Serum Test
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