• Cohen syndrome - Genetics Home Reference

    ghr.nlm.nih.gov/condition/cohen-syndrome Cohen syndrome is an inherited disorder that affects many parts of the body and is characterized by developmental delay, intellectual disability, small ...
  • Cohen Syndrome | We A.R.E. Cohen Syndrome

    cohen-syndrome.org 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 - Wikipedia, the free encyclopedia

    en.wikipedia.org/wiki/Cohen_syndrome 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 ...
    • Cohen syndrome | Counsyl

      www.counsyl.com/diseases/cohen-syndrome What is Cohen Syndrome? Cohen syndrome, also known as Pepper syndrome, is a genetic disorder that affects motor skills, mental development, and behavior.
    • Cohen Syndrome - WebMD

      www.webmd.com/children/cohen-syndrome-10577 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 ...
    • Cohen syndrome | Disease | Overview | Genetic and Rare ...

      rarediseases.info.nih.gov/gard/6126/cohen-syndrome/resources/1 A collection of disease information resources and questions answered by our Genetic and Rare Diseases Information Specialists for Cohen syndrome
    • About | Cohen Syndrome

      cohen-syndrome.org/about-2 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 - GeneReviews® - NCBI Bookshelf

      www.ncbi.nlm.nih.gov/books/NBK1482 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 - Right Diagnosis

      www.rightdiagnosis.com/c/cohen_syndrome/intro.htm Cohen Syndrome information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis.
    • Cohen syndrome – a rare genetic cause of hypotonia in children

      www.ncbi.nlm.nih.gov/pmc/articles/PMC3150073 Cohen syndrome is a rare, genetic condition, recessively inherited, associated with specific facial dysmorphism, global developmental delay, hypotonia and ophthalmic ...