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Cystinuria in Medical Dictionary

Cystinuria

... Homo cystinuria is inherited as an autosomal recessive trait, ... from both parents to be seriously affected. cystinuria is the most common defect in the transport of an ... is not the only overly excreted amino acid in cystinuria , it is the least soluble of all naturally ...

Albinism

... skin , white hair , and pink or blue eyes . Down syndrome . Homo cystinuria , a genetic condition characterized by developmental delays, failure to ... ." The 4 conditions he labeled as inborn errors were albinism , cystinuria , pentosuria and, of course, alkaptonuria . ...

Candidiasis

... ) Cyanotic Heart Disease Cystic Fibrosis Cystine Stone Disease ( cystinuria ) cystinuria ... ...

Cutaneous

... ) Cyanotic Heart Disease Cystic Fibrosis Cystine Stone Disease ( cystinuria ) cystinuria ... A vascular reaction involving the deep dermis or sub cutaneous ...

Inborn errors

... ." The 4 conditions he labeled as inborn errors were albinism , cystinuria , pentosuria and, of course, alkaptonuria . Galactosemia ... oral solution Indicated for the treatment of patients with homo cystinuria , a rare, genetic disorder caused by various inborn errors of ...

Acid

... for about six months. An amino acid found in blood and urine . Amino acid s are building blocks of protein . (See also cystine stone and cystinuria .) cystine stone: A rare form of kidney stone consisting of the amino acid cystine. Nicotinic acid ( niacin ) and bile acid sequestrants ...

Acute bilateral obstructive uropathy

... - Cancer - Cervical Cancer - Chronic Bi lateral Obstructive Uropathy - Chronic Uni lateral Obstructive Uropathy - Colon Cancer - cystinuria ... Acute bilateral obstructive uropathy Acute nephritic syndrome Bulimia Chronic kidney failure Cushing's disease Cushing's ...

Failure to thrive

... to gain weight (called failure to thrive ) Anemia (a low number of red blood cells) Fever and irritability Bone pain ... Homo cystinuria , a genetic condition characterized by developmental delays, failure to thrive , and neurological abnormalities. Turner syndrome , which causes ...

Lead Poisoning

... , and conditions outside the abdomen such as pneumonia or hip problems. Who is affected? Indications: treatment of Wilson's disease and cystinuria ; adjunctive therapy in the treatment of severe rheumatoid arthritis , lead poisoning , arsenic poisoning , and primary biliary cirrhosis . ...

Lithotripsy

... consists of a collection of tiny crystals. There can be one or more stones present at the same time in the kidney or in the ureter . (See also cystinuria .) ... lithotripsy (LITH-oh-TRIP-see): A method of breaking up kidney stones using shock waves or other means. [Top] ... lithotripsy A ...

Maple Syrup Urine Disease

... disorders can be detected by these tests, including tyrosinosis, histidinemia, maple syrup urine disease , hypervalinemia, hyperprolinemia, and homo cystinuria . ...

Nephrolithiasis

... Nephrolithiasis is a condition in which one or more stones are present in the pelvis or calyces of the kidney or in the ureter . (See also cystinuria .) Alternative Names: Renal calculi; Kidney stones ; Stones - kidney ... Nephrolithiasis : The process of forming a kidney stone, a stone ...

Poison

... ivy , poison oak, or poison sumac, and exposure to dyes used in shoes and sneakers. Indications: treatment of Wilson's disease and cystinuria ; adjunctive therapy in the treatment of severe rheumatoid arthritis , lead poison ing , arsenic poison ing , and primary biliary cirrhosis . ...

Poisoning

... 'bolt' your food - instead, eat slowly and chew thoroughly Don't eat late at night ... Indications: treatment of Wilson's disease and cystinuria ; adjunctive therapy in the treatment of severe rheumatoid arthritis , lead poisoning , arsenic poisoning , and primary biliary cirrhosis . ...

Short stature

... ... A hereditary condition characterized by sparse and brittle hair , short stature , and mental retardation . trigeminal nerve ... Homo cystinuria , a genetic condition characterized by developmental delays, failure to thrive , and neurological abnormalities. Turner syndrome , which causes ...

Trisomy

... they can also be a part of various genetic and chromosomal syndrome s, such as Down syndrome , trisomy 13 , Turner's syndrome , ... Homo cystinuria , a genetic condition characterized by developmental delays, failure to thrive , and neurological abnormalities. Turner syndrome , which causes ...
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