Paula and Bobby
Parents of Lillie
Understanding face related symptoms and features.
Symptoms may affect multiple parts of the body. Understanding which part of the body a symptom affects, can help us to better understand the potential underlying causes of a symptom, including a rare disease or genetic syndrome.
The face contains the nose, eyes and mouth, all of which are sensory organs. The face also displays emotions and feelings and plays a crucial role in communication. The face runs from the forehead at the top, to the chin at the bottom and encompasses everything in between.
Symptoms affecting the face can for the most part be seen with the naked eye. Although diagnosing a face related symptom may involve different tests and assessments, both subjective and objective.
Symptoms relating to the face may affect its structure, shape and/ or function. Some features will affect just the appearance of the face while others may affect its ability to express emotions and to communicate non-verbally.
What are Doll-like facies?
Historically this definition referred to a unique facial appearance that included a round face, accompanied by full or fat cheeks, a short and smaller nose, as well as a small chin in comparison to the rest of the face.
This definition is no longer necessarily referred to, and instead clinicians are advised to identify, measure, and diagnose each facial feature separately.
What should I do next?
In some instances, doll-like facies may be one of the features of a rare disease or genetic syndrome. In this case fast, targeted genetic analysis can give you a more accurate diagnosis.
Doll-like facial appearance
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Doll-like facial appearance
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What is FDNA Telehealth?
FDNA Telehealth is a leading digital health company that provides faster access to accurate genetic analysis.
With a hospital technology recommended by leading geneticists, our unique platform connects patients with genetic experts to answer their most pressing questions and clarify any concerns they may have about their symptoms.
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Our platform is currently used by over 70% of geneticists and has been used to diagnose over 250,000 patients worldwide.
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