How do I know if I have Cohen Syndrome?

What signs or symptoms may make you suspect you may have Cohen Syndrome. People who have experience in Cohen Syndrome offer advice of what things may make you suspicious and which doctor you should go to to receive treatment


Cohen Syndrome is a rare genetic disorder that affects multiple systems in the body. It is characterized by a combination of physical, intellectual, and developmental features. While I am not a medical professional, I can provide you with some general information about Cohen Syndrome.



Physical Features: Individuals with Cohen Syndrome often have distinct facial characteristics, such as a prominent forehead, thick eyebrows, long eyelashes, and a full lower lip. They may also have low muscle tone (hypotonia), joint hypermobility, and obesity.



Intellectual and Developmental Features: Cognitive abilities can vary widely among individuals with Cohen Syndrome. Some may have mild to moderate intellectual disability, while others may have average intelligence. Developmental delays are common, particularly in speech and motor skills. Individuals may also exhibit behavioral issues, such as attention deficit hyperactivity disorder (ADHD) or autism spectrum disorder (ASD).



Visual Impairments: Vision problems are a hallmark of Cohen Syndrome. These can include nearsightedness (myopia), astigmatism, strabismus (crossed or misaligned eyes), and progressive loss of visual acuity. Regular eye examinations are important for early detection and management of these issues.



Neutropenia: Another significant feature of Cohen Syndrome is neutropenia, which is a low level of neutrophils (a type of white blood cell). This can increase the risk of recurrent infections, particularly in the respiratory and urinary tracts.



Other Possible Features: Some individuals with Cohen Syndrome may experience hypothyroidism (underactive thyroid gland), dental abnormalities, gastrointestinal issues, and kidney problems. However, not all individuals will have these additional features.



If you suspect that you or someone you know may have Cohen Syndrome, it is crucial to consult with a healthcare professional, such as a geneticist or a pediatrician specializing in genetic disorders. They can evaluate the individual's medical history, conduct a physical examination, and order genetic testing to confirm the diagnosis.



Please remember that this information is not a substitute for professional medical advice. Only a qualified healthcare provider can accurately diagnose Cohen Syndrome based on a comprehensive evaluation.


by Diseasemaps

There are many variables with Cohen's syndrome..some are diagnosed because of chronic illnesses and blood test show lowered white blood counts and lowered Neutrophil levels ,even non existent Neutrophil levels..some are diagnosed through vision issues and some are diagnosed through genetic test because of failures in reaching child milestone markers..

9/8/17 by Melodie 2000

Genetic testing

9/8/17 by Emme 1800

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