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Hartnup Disease News, Research and Latest Updates

Keep abreast with the latest news related to Hartnup Disease there are 89 news items on Hartnup Disease that covers updates, breakthroughs and in-depth reports.

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Hartnup Disease

Hartnup disease, named after the Hartnup family in England is an inherited disorder leading to abnormal absorption and excretion of certain amino acids. The disease chiefly affects the skin and the brain.

Beat the Bellyache: Amino Acid Serine Fights Food Poisoning

Beat the Bellyache: Amino Acid Serine Fights Food Poisoning

Say goodbye to food poisoning: Amino acid serine fights back against Clostridium perfringens food poisoning.

Americans Meeting Essential Amino Acid Needs

Americans Meeting Essential Amino Acid Needs

Discover how Americans can meet their essential amino acid needs through balanced diets, promoting muscle health, energy, and overall well-being.

Extreme Heat Doubles Hospitalisation Risk for Metabolic Disorder Patients

Extreme Heat Doubles Hospitalisation Risk for Metabolic Disorder Patients

Study reveals extreme heat nearly doubles hospitalization risk for patients with metabolic disorders, including diabetes, hypertension, and obesity.

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Branched Chain Amino Acid (BCAA) Supplementation in Concussion Recovery

Branched Chain Amino Acid (BCAA) Supplementation in Concussion Recovery

Effectiveness of branched chain amino acid (BCAA) supplementation in reducing symptom severity of concussion has been revealed.

Blood Test Discovers Fetal Genetic Disorders

Blood Test Discovers Fetal Genetic Disorders

In the future, a straightforward blood test could enable the screening of pregnant women for severe genetic diseases in their unborn children.

PARMESAN: New AI Tool Revolutionizing Genetic Disorder Treatments

PARMESAN: New AI Tool Revolutionizing Genetic Disorder Treatments

PARMESAN, the natural language processing tool accelerates research, boosting drug discovery and development for scientists.

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Whole Genome Sequencing Takes the Lead in Unraveling Genetic Disorders

Whole Genome Sequencing Takes the Lead in Unraveling Genetic Disorders

Whole genome sequencing (WGS) outperforms targeted gene sequencing tests in identifying genetic disorders in newborns and infants.

How Genomic Variants Could Help Diagnose Rare Genetic Disorders

How Genomic Variants Could Help Diagnose Rare Genetic Disorders

A genotype-first approach to patient care involves selecting patients with specific genomic variants and then studying their traits and symptoms.

Kids with Rare Genetic Disorders More Likely to Suffer Other Mental Health Problems

Kids with Rare Genetic Disorders More Likely to Suffer Other Mental Health Problems

Are genetic disorders linked to developmental, behavioral and mental health problems? Routine genomic testing may hold the answer.

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Repurposed Amyotrophic Lateral Sclerosis (ALS) Drug Against Rare Genetic Disorder

Repurposed Amyotrophic Lateral Sclerosis (ALS) Drug Against Rare Genetic Disorder

Repurposed ALS (amyotrophic lateral sclerosis) drug may help slow down a rare genetic disorder in children and adolescents.

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Pellagra - Causes, Symptoms, Diagnosis, Treatment and Complications

Pellagra - Causes, Symptoms, Diagnosis, Treatment and Complications

Pellagra is a disease that occurs due to deficiency of vitamin B3 or niacin. Did you know it was first described by Don Casal a Spanish court doctor in the 18th century when skin thickening was noted in peasants.

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