Rare Diseases
The best and cost-effective real world evidence services in Rare diseases
Rare diseases require specialized research and treatment. Our services support the development of therapies for rare conditions.
Services
Marfan Syndrome
A genetic disorder affecting connective tissue, leading to long limbs, heart problems, and vision issues.
Ehlers-Danlos Syndrome
A group of connective tissue disorders causing hypermobile joints, fragile skin, and chronic pain.
Huntington’s Disease
A progressive genetic disorder that affects the brain, causing movement, cognitive, and psychiatric symptoms.
Wilson’s Disease
A rare inherited disorder causing excessive copper buildup in the liver, brain, and other organs, leading to neurological and liver damage.
Prader-Willi Syndrome
A genetic disorder causing constant hunger, obesity, developmental delays, and behavioral issues.
Angelman Syndrome
A neurogenetic disorder characterized by intellectual disability, speech impairment, balance issues, and a happy demeanor.
Tay-Sachs Disease
A fatal genetic disorder that destroys nerve cells in the brain and spinal cord, leading to progressive neurological decline.
Phenylketonuria (PKU)
A metabolic disorder where the body cannot process phenylalanine, leading to intellectual disability if untreated.
Pompe Disease
A rare genetic disorder affecting muscle function due to glycogen buildup in cells, leading to progressive weakness.
Cystinosis
A metabolic disorder causing cystine accumulation in cells, leading to kidney failure and other organ damage.
Contact us
We're here to support your research in rare diseases and enhance patients' quality of life. Contact us to explore how our services can make a significant difference in treating and understanding these unique conditions.
