Congenital dyserythropoietic anemia masquerading as hereditary spherocytosis
Background: Congenital dyserythropoietic anemias (CDA) type II is a rare hereditary chronic hemolytic anemia due to a defect in the SEC23B gene which shows varying degrees of ineffective erythropoiesis and is often misdiagnosed as a red blood cell (RBC ...
Kaninika Sanyal +4 more
core +1 more source
A novel <i>ANK1</i> gene mutation associated with hereditary spherocytosis: a case report. [PDF]
Lai M +7 more
europepmc +1 more source
Comorbidity of Dengue and Hereditary Spherocytosis in an 18-Year-Old Patient: A Case Report. [PDF]
Becerra-Carrillo RI +4 more
europepmc +1 more source
Marked reduction of spectrinin hereditary spherocytosis in the common house mouse.
In contrast to the disease in humans, hereditary spherocytosis in the common house mouse produces an extreme spherocytosis. The cells show a broad distribution in size ranging from microcytic to macrocytic.
Shohet, S B +2 more
core
Clinical Characteristics and Gene Mutations of Hereditary Spherocytosis in 59 Chinese Children. [PDF]
Li Y +7 more
europepmc +1 more source
Cognitive impairment in hereditary spherocytosis. [PDF]
Tartaglione I +12 more
europepmc +1 more source
Hereditary Spherocytosis: Linking Ion Transport Defects to Osmotic Gradient Ektacytometry Profiles-A Review. [PDF]
Vives-Corrons JL, Krishnevskaya E.
europepmc +1 more source
Hereditary Spherocytosis: Review of Presentation at Birth. [PDF]
Achenjang NS +3 more
europepmc +1 more source
Moyamoya syndrome associated with hereditary spherocytosis: pathogenesis, management, and an illustrative case with rapid radiological progression. [PDF]
Yan L, Lu X, Yang B, Ma Y.
europepmc +1 more source

