Myhre syndrome

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Editor-In-Chief: Prab R Tumpati, MD
Obesity, Sleep & Internal medicine
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Myhre syndrome
Synonyms
Pronounce
Specialty Medical genetics
Symptoms Short stature, hearing loss, intellectual disability, joint stiffness, heart defects
Complications N/A
Onset Childhood
Duration Lifelong
Types N/A
Causes Mutations in the SMAD4 gene
Risks
Diagnosis Clinical evaluation, genetic testing
Differential diagnosis Lujan–Fryns syndrome, Marfan syndrome, Loeys–Dietz syndrome
Prevention
Treatment Symptomatic and supportive
Medication
Prognosis Variable
Frequency Rare
Deaths


Myhre Syndrome is a rare genetic disorder characterized by distinctive facial features, hearing loss, and musculoskeletal abnormalities. It is caused by mutations in the SMAD4 gene and is inherited in an autosomal dominant manner.

Symptoms and Signs[edit]

Patients with Myhre Syndrome typically present with a variety of symptoms, including:

Diagnosis[edit]

The diagnosis of Myhre Syndrome is based on clinical features and confirmed by genetic testing showing a mutation in the SMAD4 gene.

Treatment[edit]

There is no cure for Myhre Syndrome. Treatment is symptomatic and supportive, and may include physical therapy for joint stiffness, hearing aids for hearing loss, and regular monitoring for cardiovascular disease.

Prognosis[edit]

The prognosis for individuals with Myhre Syndrome varies. Some individuals may have a normal lifespan, while others may have life-threatening complications due to cardiovascular disease.

See Also[edit]

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References[edit]

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External Links[edit]

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