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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.

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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 , Hypoparathyroidism : خون میں کیلشیم کی کمی , Achlorhydria : معدے میں تیزاب 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 , Dysentery : مروڑ , 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

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.

Hypoparathyroidism: inadequate secretion of parathyroid hormone resulting in abnormally low levels of calcium in the blood.

Achlorhydria: an abnormal deficiency or absence of free hydrochloric acid in the gastric juice; often associated with severe anemias and cancer of the stomach.

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.

Dysentery: an infectious disease characterized by inflammation of the intestines, leading to severe diarrhea with blood and mucus. It is typically caused by bacteria, parasites, or viruses transmitted through contaminated food or water.

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.

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