When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Methemoglobinemia - Wikipedia

    en.wikipedia.org/wiki/Methemoglobinemia

    Methemoglobinemia, or methaemoglobinaemia, is a condition of elevated methemoglobin in the blood. [2] Symptoms may include headache, dizziness, shortness of breath, nausea, poor muscle coordination, and blue-colored skin (cyanosis). [2]

  3. Hemoglobin M disease - Wikipedia

    en.wikipedia.org/wiki/Hemoglobin_M_disease

    Hemoglobin M disease is a rare form of hemoglobinopathy, characterized by the presence of hemoglobin M (HbM) and elevated methemoglobin (metHb) level in blood. [1] HbM is an altered form of hemoglobin (Hb) due to point mutation occurring in globin-encoding genes, mostly involving tyrosine substitution for proximal (F8) or distal (E7) histidine residues. [2]

  4. Methemoglobin - Wikipedia

    en.wikipedia.org/wiki/Methemoglobin

    This may be further compounded by the "functional hemoglobin's" decreased ability to release oxygen in the presence of methemoglobin. Anemia, congestive heart failure, chronic obstructive pulmonary disease, and essentially any pathology that impairs the ability to deliver oxygen may worsen the symptoms of methemoglobinemia. [9]

  5. Hemoglobinopathy - Wikipedia

    en.wikipedia.org/wiki/Hemoglobinopathy

    Diagnosis is commonly confirmed by DNA sequencing. [18] The hemoglobin structural variants can be broadly classified as follows: [19] Sickle cell disorders, which are the most prevalent form of hemoglobinopathy. Sickle hemoglobin (HbS) is prone to polymerize when deoxygenated, precipitating within the red blood cell. This damages the RBC ...

  6. Blue baby syndrome - Wikipedia

    en.wikipedia.org/wiki/Blue_baby_syndrome

    A methemoglobin level > 1.5 g/dL causes cyanosis. The most common congenital cause is a deficiency in the enzyme cytochrome b5 reductase which reduces methemoglobin in the blood. [22] However, in infants the most common cause of methemoglobinemia is acquired through the ingestion of nitrates (NO − 3) through well water or foods.

  7. Cytochrome b5 reductase - Wikipedia

    en.wikipedia.org/wiki/Cytochrome_b5_reductase

    Due to the lack of oxygen that can be carried by the RBCs, symptoms include a bluish appearance of the skin, lips, and nails . This is the most common variation of a c5br mutation. The type I variation of methemoglobinemia is the first category out of two congenital, autosomal recessive disorders resulting from mutations of the c5br gene. While ...

  8. Blue Fugates - Wikipedia

    en.wikipedia.org/wiki/Blue_Fugates

    The disorder can cause heart abnormalities and seizures if the amount of methemoglobin in the blood exceeds 20 percent, but at levels between 10 and 20 percent it can cause blue skin without other symptoms. Most of the Fugates lived long and healthy lives. The "bluest" of the blue Fugates, Luna Stacy, had 13 children and lived to age 84. [6]

  9. Hemoglobinemia - Wikipedia

    en.wikipedia.org/wiki/Hemoglobinemia

    Hemoglobinemia (or haemoglobinaemia) is a medical condition in which there is an excess of hemoglobin in the blood plasma.This is an effect of intravascular hemolysis, in which hemoglobin separates from red blood cells, a form of anemia.