Abetalipoproteinemia meaning in Urdu
Abetalipoproteinemia Definitions
1) Abetalipoproteinemia : خون کی موروثی بیماری : (noun) a rare inherited disorder of fat metabolism; characterized by severe deficiency of beta-lipoproteins and abnormal red blood cells (acanthocytes) and abnormally low cholesterol levels.
Useful Words
Acanthocytosis : خون میں خراب خلیوں کی موجودگی , Hepatolenticular Degeneration : خون میں تانبے کی بیماری , Hdl Cholesterol : اچھی چکنائی , Albers-Schonberg Disease : مرمری ہڈیاں , Diabetes : پیشاب میں شکر آنا , Alpha-Lipoprotein : اعلی کثافت کی لیپوپروٹین , Agammaglobulinemia : مدافعتی کمزوری , Agranulocytosis : گرینولوسائیٹس کی کمی , Anaemia : خون کی کمی , Lovastatin : خون سے کولیسٹرال کم کرنے کی دوا , Achlorhydria : معدے میں تیزاب کی کمی , Hypoparathyroidism : خون میں کیلشیم کی کمی , Hypocalcaemia : خون میں کیلسیم کی مقدار کا کم ہونا , Thrombocytopenia : خون میں پلیٹلیٹ کی تعداد میں تخفیف , Hypercalcaemia : خون میں کیلشیم کی زیادتی , Acidemia : خون میں تیزابیت , High Blood Pressure : بلند فشار خون , Acetoacetic Acid : خون میں شامل تیزاب , Histiocytosis : خون کی بیماری , Lipid Profile : کولیسٹرول کا ٹیسٹ , Anorexia : بھوک کی کمی , Diapedesis : بافتوں میں رگوں کی دیواروں میں سے خونی خلیوں کا گزرنا , Cancer Of The Blood : خون کا سرطان , Glycosuria : پیشاب میں پائی جانے والی شکر , Glucagon : لبلبہ کے آئیلٹس آف لنگرہانز کے الفا خلیوں میں پیدا ہونے والا ہارمون , Xanthoma : جلد کے نیچے کولیسٹرول کا مجموعہ , Acute Lymphoblastic Leukemia : خون کے سرطان کی شدید قسم , Rachitis : بچوں میں وٹامن ڈی کی کمی , Blood Group : خون کا گروپ , Moon Blindness : رات کے وقت کم نظر آنا , Hypercalcinuria : پیشاب میں کیلشیم کی زیادہ مقدار
Useful Words Definitions
Acanthocytosis: the presence of acanthocytes in the blood stream (as in abetalipoproteinemia).
Hepatolenticular Degeneration: a rare inherited disorder of copper metabolism; copper accumulates in the liver and then in the red blood cells and brain.
Hdl Cholesterol: the cholesterol in high-density lipoproteins; the `good` cholesterol; a high level in the blood is thought to lower the risk of coronary artery disease.
Albers-Schonberg Disease: an inherited disorder characterized by an increase in bone density; in severe forms the bone marrow cavity may be obliterated.
Diabetes: a polygenic disease characterized by abnormally high glucose levels in the blood; any of several metabolic disorders marked by excessive urination and persistent thirst.
Alpha-Lipoprotein: a lipoprotein that transports cholesterol in the blood; composed of a high proportion of protein and relatively little cholesterol; high levels are thought to be associated with decreased risk of coronary heart disease and atherosclerosis.
Agammaglobulinemia: a rare immunological disorder characterized by the virtual absence of gamma globulin in the blood and consequent susceptibility to infection.
Agranulocytosis: an acute blood disorder (often caused by radiation or drug therapy) characterized by severe reduction in granulocytes.
Anaemia: Anemia is a medical condition characterized by a decrease in the number of red blood cells or a low concentration of hemoglobin in the blood. Hemoglobin is the protein in red blood cells responsible for carrying oxygen from the lungs to the body`s tissues. When the level of hemoglobin or red blood cells falls below the normal range, it can lead to a reduced ability of the blood to carry oxygen effectively.
Lovastatin: an oral drug (trade name Mevacor) to reduce blood cholesterol levels; used when dietary changes have proved inadequate.
Achlorhydria: an abnormal deficiency or absence of free hydrochloric acid in the gastric juice; often associated with severe anemias and cancer of the stomach.
Hypoparathyroidism: inadequate secretion of parathyroid hormone resulting in abnormally low levels of calcium in the blood.
Hypocalcaemia: abnormally low level of calcium in the blood; associated with hypoparathyroidism or kidney malfunction or vitamin D deficiency.
Thrombocytopenia: a blood disease characterized by an abnormally small number of platelets in the blood.
Hypercalcaemia: the presence of abnormally high levels of calcium in the blood; usually the result of excessive bone resorption in hyperparathyroidism or Paget's disease.
Acidemia: a blood disorder characterized by an increased concentration of hydrogen ions in the blood (which falls below 7 on the pH scale).
High Blood Pressure: a common disorder in which blood pressure remains abnormally high (a reading of 140/90 mm Hg or greater).
Acetoacetic Acid: unstable acid found in abnormal amounts in the blood and urine in some cases of impaired metabolism (as diabetes mellitus or starvation).
Histiocytosis: a blood disease characterized by an abnormal multiplication of macrophages.
Lipid Profile: A lipid profile, also known as a lipid panel or lipid profile test, is a blood test that measures various types of lipids (fats) in the bloodstream. It provides important information about a person`s cholesterol levels and other lipid-related factors, which are significant indicators of cardiovascular health.
Anorexia: a psychological disorder characterized by a severe fear of gaining weight, leading to self-imposed starvation, extreme thinness, and an obsessive preoccupation with food, dieting, and body image.
Diapedesis: passage of blood cells (especially white blood cells) through intact capillary walls and into the surrounding tissue.
Cancer Of The Blood: malignant neoplasm of blood-forming tissues; characterized by abnormal proliferation of leukocytes; one of the four major types of cancer.
Glycosuria: the presence of abnormally high levels of sugar in the urine.
Glucagon: a hormone secreted by the pancreas; stimulates increases in blood sugar levels in the blood (thus opposing the action of insulin).
Xanthoma: a skin problem marked by the development (on the eyelids and neck and back) of irregular yellow nodules; sometimes attributable to disturbances of cholesterol metabolism.
Acute Lymphoblastic Leukemia: acute leukemia characterized by proliferation of immature lymphoblast-like cells in bone marrow, lymph nodes, spleen, and blood; most common in children.
Rachitis: childhood disease caused by deficiency of vitamin D and sunlight associated with impaired metabolism of calcium and phosphorus.
Blood Group: human blood cells (usually just the red blood cells) that have the same antigens.
Moon Blindness: inability to see clearly in dim light; due to a deficiency of vitamin A or to a retinal disorder.
Hypercalcinuria: the presence of abnormally high levels of calcium in the urine; usually the result of excessive bone resorption in hyperparathyroidism or osteoporosis.