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Inborn Errors of Metabolism News, Research and Latest Updates

Keep abreast with the latest news related to Inborn Errors of Metabolism there are 356 news items on Inborn Errors of Metabolism that covers updates, breakthroughs and in-depth reports.

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Inborn Errors of Metabolism

Inborn errors of metabolism are genetic disorders that hamper the body’s metabolism resulting in severe clinical manifestations.

Next-Gen Nasal Spray Gene Therapy Targets Lung Diseases and COVID-19

Next-Gen Nasal Spray Gene Therapy Targets Lung Diseases and COVID-19

A new nasal spray-based gene therapy, using AAV.CPP.16 shows promise for treating lung diseases like COVID-19 and pulmonary fibrosis.

Early Menopause Raises Risk of Fatty Liver and Metabolic Disorders

Early Menopause Raises Risk of Fatty Liver and Metabolic Disorders

Early menopause is linked to higher risk of fatty liver disease and metabolic complications in women.

India Takes Historic Step With First Gene Therapy for Hemophilia

India Takes Historic Step With First Gene Therapy for Hemophilia

India has launched its first human gene therapy for hemophilia, showing progress in biotech-led healthcare innovation.

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Gene Therapy for Maple Syrup Urine Disease: A Promising New Approach

Gene Therapy for Maple Syrup Urine Disease: A Promising New Approach

Gene therapy offers new hope for treating Maple Syrup Urine Disease, a rare metabolic disorder, by addressing its root cause for potential long-term relief.

Inhalable Gene Therapy Trialed for Cystic Fibrosis Patients

Inhalable Gene Therapy Trialed for Cystic Fibrosis Patients

Researchers trial inhalable gene therapy for cystic fibrosis, offering a potential breakthrough in treating the genetic lung disease.

AAV-Based Gene Therapy for Chronic hypereosinophilia

AAV-Based Gene Therapy for Chronic hypereosinophilia

Discover how AAV-based gene therapy delivers anti-eosinophil antibodies, offering hope for chronic hypereosinophilia treatment

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India’s Medical Milestone: Gene Therapy Success for Haemophilia A

India’s Medical Milestone: Gene Therapy Success for Haemophilia A

Integrated gene therapy successfully treated Haemophilia A in India, providing long-term relief without bleeding episodes for over 14 months, signaling a potential cure.

Speed Matters: How Walking Fast Helps Prevent Metabolic Disorders

Speed Matters: How Walking Fast Helps Prevent Metabolic Disorders

Can walking speed reveal health risks in obesity? Yes, a quicker pace reduces the chances of diabetes, hypertension, and more, according to a recent study.

Better Than Fine: Sickle Cell's First Base Editing Gene Therapy Success Story

Better Than Fine: Sickle Cell's First Base Editing Gene Therapy Success Story

Sickle cell treatment: Base editing gene therapy is rewriting the future for sickle cell patients, leaving them healthier and pain-free.

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Gene Therapy Converts Omega-6 to Omega-3 Fatty Acids to Combat Arthritis

Gene Therapy Converts Omega-6 to Omega-3 Fatty Acids to Combat Arthritis

Gene therapy converts harmful Omega-6 fatty acids to beneficial Omega-3s, reducing childhood obesity and arthritis risk.

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Recommended Reading

Galactosemia - Genetic Disorder of Sugar Galactose

Galactosemia - Genetic Disorder of Sugar Galactose

Galactosemia is one of many genetically inherited diseases and it affects one’s ability to process galactose. Learn about the symptoms, diagnosis and treatment for galactosemia.

Mucopolysaccharidosis | Inborn Metabolic Diseases - Types, Symptoms, Diagnosis, Treatment

Mucopolysaccharidosis | Inborn Metabolic Diseases - Types, Symptoms, Diagnosis, Treatment

Mucopolysaccharidosis (MPS) are a group of inborn metabolic disorders due to the absence or malfunctioning of specific enzymes required to process molecules called glycosaminoglycans.

Metabolic Defects - Phenylketonuria

Metabolic Defects - Phenylketonuria

Encyclopedia section of medindia gives information regarding Phenylketonuria type of Metabolic defect

Alkaptonuria (Black Urine Disease) - Causes, Symptoms, Diagnosis, Treatment and Prognosis

Alkaptonuria (Black Urine Disease) - Causes, Symptoms, Diagnosis, Treatment and Prognosis

Alkaptonuria or black urine disease is an inherited disorder where a chemical called homogentisic acid accumulates in the tissues and body fluids staining them dark brown. The spine and large joints (hip, knee) are affected leading to pain and stiffness.

Homocystinuria | Amino Acid Metabolism Disorder - Causes, Symptoms, Diagnosis and Treatment

Homocystinuria | Amino Acid Metabolism Disorder - Causes, Symptoms, Diagnosis and Treatment

Homocystinuria is a rare inherited condition characterized by increased levels of the amino acid homocysteine in the blood and urine. Early diagnosis and treatment is important to avoid serious complications later

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