Phenylalanine in Medical Dictionary

Metabolize

... the body cannot metabolize a protein c alled phenylalanine . It is estimated that one baby in 10,000 to ... disorder. Causes an inability to metabolize phenylalanine , an amino acid that's a common part of many ... foods that contain large amounts of phenylalanine , one of the ingredients in aspartame. People ...

Phenylalanine

... phenylalanine : An essential amino acid . (The human body cannot make it so it is essential to the diet .) phenylalanine that is ingested is largely transformed ... which is used in protein s ynthesis. phenylalanine ; ...

Phenylketonuria

... recessive manner, as are lesser degrees of phenylalanine hydroxylase deficiency . Phenylketonuria is ... the body cannot metabolize a protein c alled phenylalanine . It is estimated that one baby in 10,000 to ... disorder. Causes an inability to metabolize phenylalanine , an amino acid that's a common part of many ...

Pku

... caused by the absence of a specific enzyme ( phenylalanine hydroxylase). The absence of this enzyme , a ... trait, prevents the body from making use of phenylalanine ... PKU is a genetic disorder with a ... the body cannot metabolize a protein c alled phenylalanine . It is estimated that one baby in 10,000 to ...

Protein

... that relieves pain . Aspirin and acetaminophen are mild analgesics. phenylalanine is present in high protein foods . After the body has absorbed enough for its needs, an enzyme normally converts some phenylalanine to tyrosine, another essential amino acid ; in PKU , however, that ...

Acid

... dichloroacetic acid ) topically to treat plantar warts . After the body has absorbed enough for its needs, an enzyme normally converts some phenylalanine to tyrosine, another essential amino acid ; in PKU , however, that vital enzyme is absent or insufficient, so conversion to tyrosine does not ...

Aspartic acid

... alanine, arginine, asparagine, aspartic acid , cysteine, glutamic acid , glutamine, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine , proline, serine, threonine, tryptophan , tyrosine, and valine. ...

Autosomal recessive

... A mutation in a single gene causes PKU . This gene contains the instructions for making an enzyme needed to process the amino acid called phenylalanine . Amino acids are the building blocks for protein . Autosomal recessive inheritance Supportive treatment Normally the cerebellum (an area ...

Cavity

... result from the spinal cord damage. The cavity of the canal leading from the mouth and nasal passages to the larynx and the esophagus . phenylalanine ... Intra cavity radiation often is used for gynecologic cancer s. Under general or spinal anesthesia , hollow applicators are placed directly ...

Enzyme

... protective effect on the kidney in people with diabetes . After the body has absorbed enough for its needs, an enzyme normally converts some phenylalanine to tyrosine, another essential amino acid ; in PKU , however, that vital enzyme is absent or insufficient, so conversion to tyrosine does not ...

Fructose

... fruits, especially figs, dates, prunes, pears and grapes. It's also found in smaller amounts in onions, asparagus, artichokes and wheat. borono phenylalanine - fructose complex BPA-F. A substance used in a type of radiation therapy called boron neutron capture therapy. BPA-F is injected into a vein , ...

Growth Charts

... Does the child eat well? Your doctor will determine a safe amount through regular review of diet records, growth charts and blood levels of phenylalanine . This is sometimes known as constitutional short stature and, of course, no treatment is needed. What's important is that the child is ...

Pharynx

... that line the oro pharynx . pharynx The cavity of the canal leading from the mouth and nasal passages to the larynx and the esophagus . phenylalanine ... pharynx (FAIR-inks) The hollow tube about 5 inches long that starts behind the nose and ends at the top of the trachea (windpipe) and ...

Protein S

... plate and meat or non-meat protein s hould take up another 1/4 of the plate. (The human body cannot make it so it is essential to the diet .) phenylalanine that is ingested is largely transformed (hydroxylated) to form the amino acid tyrosine, which is used in protein s ynthesis. The term albumin ...

Tryptophan

... alanine, arginine, asparagine, aspartic acid , cysteine, glutamic acid , glutamine, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine , proline, serine, threonine, tryptophan , tyrosine, and valine. Some researchers believe that anorexia and bulimia are caused by chemical ...

Tyrosinemia

... feed. It also appears to be common in premature babies. Orfadin (nitisinone) capsules Indication: Adjunct to dietary restriction of tyrosine and phenylalanine for the treatment of hereditary tyrosinemia type 1 (HT-1). Mfg: Orphan Pharmaceuticals USA. Being male. Having hepatitis B or hepatitis C ....