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  • Hereditary Spherocytosis: Symptoms, Causes Treatment
    Hereditary spherocytosis (HS) is an inherited blood disorder that causes hemolytic anemia Hemolytic anemia is a term that describes the premature breakdown of red blood cells
  • Spherocytosis - Wikipedia
    Spherocytosis is the presence of spherocytes in the blood, i e erythrocytes (red blood cells) that are sphere-shaped rather than bi-concave disk shaped as normal
  • Hereditary Spherocytosis - StatPearls - NCBI Bookshelf
    Membrane loss results in spherocytosis, a drop in mean corpuscular volume (MCV), an increase in mean corpuscular hemoglobin concentration (MCHC), and increased osmotic fragility of RBCs Spherocytes are destroyed and cleared from circulation during passage through the spleen
  • Hereditary Spherocytosis | Symptoms, Diagnosis Treatment
    Hereditary spherocytosis is a disorder that affects the red blood cells Read about causes, symptoms, diagnosis and treatment of spherocytosis in children
  • What Is Hereditary Spherocytosis? Causes Treatment
    Hereditary spherocytosis causes fragile, sphere-shaped red blood cells that break down too easily Learn about symptoms, complications, and treatment options
  • Hereditary spherocytosis: MedlinePlus Genetics
    Hereditary spherocytosis is a condition that affects red blood cells People with this condition typically experience a shortage of red blood cells (anemia), yellowing of the eyes and skin (jaundice), and an enlarged spleen (splenomegaly)
  • Hereditary Spherocytosis Symptoms and Treatment - Verywell Health
    Spherocytosis, otherwise known as hereditary spherocytosis, is an inherited blood disorder that causes red blood cells to become sphere-shaped (spherocytes) rather than their normal disk shape Symptoms include jaundice, fatigue, shortness of breath, and a swollen abdomen due to an enlarged spleen 1 2
  • Spherocytosis - Ask Hematologist | Understand Hematology
    Hereditary spherocytosis (HS) is the most common inherited red blood cell membrane disorder, typically transmitted in an autosomal dominant pattern It is characterized by structurally abnormal red blood cells that become spherical (spherocytes), rigid, and osmotically fragile


















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