Freeman–Sheldon syndrome

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Freeman-Sheldon syndrome

Freeman–Sheldon syndrome (FSS), also known as whistling face syndrome, is a rare congenital disorder characterized by multiple physical abnormalities. It is named after the American pediatrician Ernest Arthur Freeman and the British orthopedic surgeon Joseph Harold Sheldon, who first described the syndrome in 1938.

Clinical Features[edit | edit source]

Individuals with Freeman–Sheldon syndrome typically present with distinctive facial features, including a small mouth (microstomia), pursed lips, deep-set eyes, and a prominent forehead. These facial characteristics often give the appearance of a "whistling face." Other common features include:

Genetics[edit | edit source]

Freeman–Sheldon syndrome is usually inherited in an autosomal dominant manner, although cases of autosomal recessive inheritance have also been reported. The condition is associated with mutations in the MYH3 gene, which encodes a protein involved in muscle contraction.

Diagnosis[edit | edit source]

Diagnosis of Freeman–Sheldon syndrome is primarily based on clinical evaluation and the presence of characteristic physical features. Genetic testing can confirm the diagnosis by identifying mutations in the MYH3 gene.

Management[edit | edit source]

There is no cure for Freeman–Sheldon syndrome, and treatment is focused on managing symptoms and improving quality of life. This may include:

Prognosis[edit | edit source]

The prognosis for individuals with Freeman–Sheldon syndrome varies depending on the severity of the condition and the presence of associated complications. With appropriate medical care and supportive therapies, many individuals can lead relatively normal lives.

Related Pages[edit | edit source]

References[edit | edit source]

External Links[edit | edit source]


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Contributors: Prab R. Tumpati, MD