Science, asked by chitragharge, 4 months ago

Phenylketonuria: Gene theraphy:: Polio: ? co relate the terms

raidyraidy: NVM

Dikshant2005: lmao

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raidyraidy: goodmorning

chitragharge: I want answer of.. phenylketonuria:gene therapy:: polio:??

Dikshant2005: morning

Dikshant2005: Phenylketonuria (PKU) is an inborn error of metabolism that results in decreased metabolism of the amino acid phenylalanine. Untreated, PKU can lead to intellectual disability, seizures, behavioral problems, and mental disorders. It may also result in a musty smell and lighter skin.

raidyraidy: i will gotta go i have quiz Math

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Answers

Answered by Dikshant2005

Answer:

Prekulab’s innovative range of tablets and powders allows you to live a more ordinary life with phenylketonuria (PKU). With our clinically-proven Large Neutral Amino Acid formulations PreKUnil and NeoPhe, up to 80% of your protein intake can be from normal food, and you can feel in control of your PKU. Be who you want to be, live how you want to live, and don’t let anything hold you back.

NeoPhe Tablets and Powder

Our newest and most advanced LNAA product gives double protection from Phe, stopping it from entering the brain and also inhibiting entry to the blood. Clinically proven NeoPhe is available in odour and flavourless tablets and citrus-flavoured powder, and allows PKU patients to get up to 80% of their protein intake from a normal diet.

PreKUnil Tablets

This advanced product pioneered the use of LNAAs in the treatment of phenylketonuria. It has been successful for PKU patients for more than 30 years. It is clinically proven to reduce Phe transport across the blood-brain barrier. PreKUnil allows PKU patients to get up to 80% of their protein intake from a normal diet. It is also suitable for late-diagnosed and untreated PKU.

Avonil Tablets and Powder

A conventional method for the management of PKU, Avonil contains all essential amino acids except Phe, plus multiple vitamins and minerals. Tablets are formulated for easy swallowing, while the powder is mixed with water or juice to drink. Tablets and powder are suitable for all ages, including children and during pregnancy, and must be combined with a restricted diet.

Case stories

Find out how Prekulab’s products have empowered people with PKU to live the life they want.

“

Now my daughter has

more opportunities to

do normal things. People

see Astrid first, and then

PKU.

Bodil Højgaard

Astrid’s mother

“

I feel like I’m in control

of my PKU, not the other

way around, I sometimes

even forget I have it.

Laura Momme

Student

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raidyraidy: Classical phenylketonuria (PKU) is an autosomal recessive disorder caused by a deficiency of hepatic phenylalanine hydroxylase (PAH).

raidyraidy: hanggang dyan lng lodi

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