Cohen syndrome is an inherited disorder that affects many parts of the body and is characterized by developmental delay, intellectual disability, small ...
Cohen Syndrome is a rare genetic disorder associated with mutations present at COH1 within chromosome 8 and is often undiagnosed for many years.
Cohen syndrome (also known as Pepper syndrome or Cervenka syndrome, named after Michael Cohen, William Pepper and Jaroslav Cervenka, who researched the illness) is a ...
What is Cohen Syndrome? Cohen syndrome, also known as Pepper syndrome, is a genetic disorder that affects motor skills, mental development, and behavior.
Important It is possible that the main title of the report Cohen Syndrome is not the name you expected. Please check the synonyms listing to find the ...
A collection of disease information resources and questions answered by our Genetic and Rare Diseases Information Specialists for Cohen syndrome
Company Overview: Founded in 2008. We are a 501(C)(3) non-profit association founded by parents of Cohen Syndrome children. We are a 100% volunteer organization that ...
Cohen syndrome is characterized by failure to thrive in infancy and childhood; truncal obesity in the teen years; early-onset hypotonia and developmental delays ...
Cohen Syndrome information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis.
Cohen syndrome is a rare, genetic condition, recessively inherited, associated with specific facial dysmorphism, global developmental delay, hypotonia and ophthalmic ...