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Farber disease News, Research and Latest Updates

Keep abreast with the latest news related to Farber disease there are 54 news items on Farber disease that covers updates, breakthroughs and in-depth reports.

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Farber disease

Farber disease is a genetic disease characterised by the deficiency of ceramidase. It has no specific treatment.

New Genetic Disease That Delays Brain Development in Children Discovered

New Genetic Disease That Delays Brain Development in Children Discovered

A novel genetic disease drives some kids' brains to develop abnormally, resulting in delayed intellectual development.

Mechanism Involved in Transmission of Genetic Disease from Mother to Child

Mechanism Involved in Transmission of Genetic Disease from Mother to Child

A new mechanism discovered by scientists helps explain how mitochondrial diseases are transmitted from mother to child.

Lethal Genetic Disease Might Be Efficiently Treated Using Gene Editing

Lethal Genetic Disease Might Be Efficiently Treated Using Gene Editing

Scientists developed prenatal genetic editing as an efficient treatment for lysosomal storage disease in a preclinical model.

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Manuka Honey Kills Drug-resistant Bacteria in Genetic Disease

Manuka Honey Kills Drug-resistant Bacteria in Genetic Disease

Manuka honey could provide the breakthrough treatment for cystic fibrosis patients who suffer from frequent infections.

AI can Identify Risk of Genetic Disease Causing High Cholesterol

AI can Identify Risk of Genetic Disease Causing High Cholesterol

New artificial intelligence (AI) based technology can accurately identify patients with familial hypercholesterolemia (FH), a rare genetic disease that causes elevated blood cholesterol levels.

Phenylketonuria, the Genetic Disease Healed Using Genome Editing

Phenylketonuria, the Genetic Disease Healed Using Genome Editing

Phenylketonuria, a birth defect that increases the levels of a substance called phenylalanine in the blood is healed using CRISPR/Cas9 system.

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Scientists Identify Cause of AEC Syndrome, a Severe Genetic Disease

Scientists Identify Cause of AEC Syndrome, a Severe Genetic Disease

Mutations in the p63 protein lead to a number of disorders including AEC syndrome.

Many Patients Carry Rare Genetic Disease Risks

Many Patients Carry Rare Genetic Disease Risks

In the world, every 60 seconds, ten children are born who will suffer from one of the more than six thousand rare genetic diseases that, to date, we know exist.

Mechanism Behind Rare Genetic Disease in Babies Revealed

Mechanism Behind Rare Genetic Disease in Babies Revealed

Hyaline Fibromatosis Syndrome caused by gene mutations of CMG2 interacts with a type of collagen found in skin, cartilage, blood vessels and teeth.

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Facial Recognition Software Helps to Diagnose Rare Genetic Disease

Facial Recognition Software Helps to Diagnose Rare Genetic Disease

A facial recognition software can be used to diagnose rare genetic disease, finds study.

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Recommended Reading

About Genetic Testing

About Genetic Testing

Genetic testing helps to confirm a genetic condition in an individual and involves q complex laboratory techniques

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