Leukodystrophy describes a group of more than 50 rare, inherited neurological disorders.
People with (MSUD) can’t break down three specific amino acids found in protein-containing foods.
Is a rare inherited disorder that causes an amino acid called phenylalanine to build up in the body.
is a rare genetic condition that occurs when your body accumulates too much copper, especially in the liver and brain.
Haemochromatosis is an inherited condition where iron levels in the body slowly build up over many years.
Mitochondrial diseases are a group of genetic conditions that affect how mitochondria in your cells produce energy.
Hyperlipidemia (high cholesterol) is an excess of lipids or fats in your blood.
Charcot-Marie-Tooth disease (CMT) is a group of genetic conditions that affect the nerves connecting the brain and spinal cord to the rest of the body.
Is a chronic (long-term) digestive and immune disorder that damages your small intestine.
The damage may prevent your body from absorbing vitamins, minerals, and other nutrients from the food you eat.
Lactose is a type of sugar found in milk and other dairy products.
An enzyme called lactase is needed by the body to digest lactose.
Gaucher disease is a rare, inherited condition that leads to the buildup of a fatty substance in tissue
This buildup causes damage and dysfunction of tissues and organs. The spleen, liver and bones are most often affected.
Amyloidosis is a rare disease that occurs when a protein called amyloid builds up in organs.
This amyloid buildup can affect the way organs work.
Metabolic syndrome is a group of conditions that increase the risk of heart disease, stroke and type 2 diabetes.
These conditions include high blood pressure, high blood sugar, too much fat around the waist, and high cholesterol or triglyceride levels.
It’s common to get a little constipated if you don’t drink enough water.
Inactivity, diet changes, illness, and even stress can add to the problem.
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