Keyword Analysis & Research: pku disease

Keyword Analysis

Keyword	CPC	PCC	Volume	Score	Length of keyword
pku disease	0.89	0.2	3162	67	11
pku	1.33	0.6	3603	83	3
disease	0.39	0.6	4488	1	7

Keyword	CPC	PCC	Volume	Score
pku disease	0.46	0.6	8842	5
pku disease diet	1.28	0.5	8608	39
pku disease symptoms	0.54	0.9	1662	22
pku disease treatment	0.39	0.8	1032	87
pku disease in adults	0.21	0.2	7011	52
pku disease baby	0.95	0.5	4305	76
pku disease pictures	0.33	0.3	5234	30
pku disease life expectancy	1.44	0.1	5258	96
pku disease slideshare	0.69	0.3	2762	89
pku disease in children	1.2	0.4	4625	35
pku disease is autosomal recessive	1.64	1	7319	14
pku disease nhs	0.48	0.8	2486	70
pku disease blood	1.73	0.5	5003	28
what is pku disease	0.77	0.4	6363	32
pku tests for what diseases	0.77	1	1417	85
what kind of disease pku is	1.85	0.8	7718	25
when do newborns with pku show disease	0.02	0.2	9386	59
what causes pku disease	0.52	0.1	3342	51
is pku a rare disease	1.16	0.4	2069	58
famous people with pku disease	1.06	0.5	30	53

Phenylketonuria (PKU) - Symptoms and causes - Mayo Clinic
mayoclinic.org

https://www.mayoclinic.org/diseases-conditions/phenylketonuria/symptoms-causes/syc-20376302

WEBMay 13, 2022 · Phenylketonuria (fen-ul-key-toe-NU-ree-uh), also called PKU, is a rare inherited disorder that causes an amino acid called phenylalanine to build up in the body. PKU is caused by a change in the phenylalanine hydroxylase (PAH) gene. This gene helps create the enzyme needed to break down phenylalanine.

DA: 22 PA: 1 MOZ Rank: 4

Phenylketonuria - Wikipedia
wikipedia.org

https://en.wikipedia.org/wiki/Phenylketonuria

WEBPhenylketonuria ( PKU) is an inborn error of metabolism that results in decreased metabolism of the amino acid phenylalanine. [3] . Untreated PKU can lead to intellectual disability, seizures, behavioral problems, and mental disorders. [1] [7] It may also result in a musty smell and lighter skin. [1] .

DA: 90 PA: 8 MOZ Rank: 40

Phenylketonuria (PKU): Symptoms, Causes & Treatment
clevelandclinic.org

https://my.clevelandclinic.org/health/diseases/17816-phenylketonuria

WEBAug 15, 2022 · Phenylketonuria (PKU) is a genetic condition that causes elevated levels of a substance called phenylalanine to build up in your body. Phenylalanine is found in the body as part of normal biochemical pathways, but problems arise when levels are persistently higher than normal.

DA: 45 PA: 71 MOZ Rank: 31

Phenylketonuria (PKU) - Diagnosis and treatment - Mayo Clinic
mayoclinic.org

https://www.mayoclinic.org/diseases-conditions/phenylketonuria/diagnosis-treatment/drc-20376308

WEBMay 13, 2022 · Request an Appointment. Symptoms & causes. Diagnosis & treatment. Diagnosis. Newborn screening identifies almost all cases of phenylketonuria. All 50 states in the United States require newborns to be screened for PKU. Many other countries also routinely screen infants for PKU.

DA: 94 PA: 36 MOZ Rank: 42

Phenylketonuria: Causes, Symptoms, and Diagnosis - Healthline
healthline.com

https://www.healthline.com/health/phenylketonuria

WEBJul 25, 2017 · Phenylketonuria (PKU) Symptoms. Causes. Diagnosis. Treatments. In pregnancy. Outlook. Prevention. What is phenylketonuria? Phenylketonuria (PKU) is a rare genetic condition that causes an...

DA: 86 PA: 4 MOZ Rank: 88

Phenylketonuria (PKU) - NICHD - Eunice Kennedy Shriver …
nih.gov

https://www.nichd.nih.gov/health/topics/factsheets/pku

WEBMay 15, 2012 · Phenylketonuria, often called PKU, is an inherited disorder that can cause intellectual and developmental disabilities (IDDs) if not treated. In PKU, the body can’t process a portion of a protein called phenylalanine, which is in all foods containing protein.

DA: 16 PA: 61 MOZ Rank: 100

Quick Facts: Phenylketonuria (PKU) - Merck Manuals Consumer Version
merckmanuals.com

https://www.merckmanuals.com/home/quick-facts-children-s-health-issues/hereditary-metabolic-disorders/phenylketonuria-pku

WEBWhat is phenylketonuria (PKU)? What causes PKU? What are the symptoms of PKU? How can doctors tell if my child has PKU? How do doctors treat PKU? What is phenylketonuria (PKU)? Phenylketonuria is a hereditary metabolic disorder . Children with PKU are born without the enzyme needed to break down phenylalanine.

DA: 60 PA: 24 MOZ Rank: 31

About Phenylketonuria - National Human Genome Research …
genome.gov

https://www.genome.gov/Genetic-Disorders/Phenylketonuria

WEBAug 21, 2014 · Phenylketonuria (PKU) is an inherited disorder of metabolism that causes an increase in the blood of a chemical known as phenylalanine. Phenylalanine comes from a person's diet and is used by the body to make proteins. Phenylalanine is found in all food proteins and in some artificial sweeteners. Without dietary treatment, phenylalanine can ...

DA: 46 PA: 78 MOZ Rank: 75

Phenylketonuria (PKU) - Diagnosis - Mayo Clinic
mayoclinic.org

https://www.mayoclinic.org/diseases-conditions/phenylketonuria/diagnosis-treatment/diagnosis/dxc-20376303

WEBMay 13, 2022 · PKU is caused by a change in the gene that helps create an enzyme needed to break down phenylalanine. Treatment includes a special diet and medication. Learn more about services at Mayo Clinic.

DA: 32 PA: 43 MOZ Rank: 5

Phenylketonuria - NHS
www.nhs.uk

https://www.nhs.uk/conditions/phenylketonuria/

WEBPage last reviewed: 04 April 2023. Next review due: 04 April 2026. Find out about phenylketonuria (PKU), a rare genetic condition that's present from birth (congenital), where the body is unable to break down phenylalanine.

DA: 82 PA: 66 MOZ Rank: 21