Nasodigitoacoustic syndrome

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Nasodigitoacoustic syndrome is a rare genetic disorder characterized by a combination of distinctive facial features, digital anomalies, and hearing impairment. The syndrome is also known as Keipert syndrome, named after the researcher who first described it.

Clinical Features

Individuals with Nasodigitoacoustic syndrome typically present with the following clinical features:

• Facial dysmorphism: This includes a broad nasal bridge, a bulbous nasal tip, and a long philtrum.
• Digital anomalies: These may include brachydactyly (short fingers), clinodactyly (curved fingers), and syndactyly (webbed fingers or toes).
• Hearing impairment: Affected individuals often have sensorineural hearing loss, which can range from mild to severe.

Genetics

Nasodigitoacoustic syndrome is believed to follow an autosomal dominant inheritance pattern. This means that a single copy of the altered gene in each cell is sufficient to cause the disorder. The specific gene or genes involved in Nasodigitoacoustic syndrome have not yet been identified.

Diagnosis

The diagnosis of Nasodigitoacoustic syndrome is primarily based on clinical evaluation and the presence of characteristic features. Genetic testing may be used to confirm the diagnosis and to differentiate it from other syndromes with overlapping features.

Management

There is no cure for Nasodigitoacoustic syndrome, and treatment is symptomatic and supportive. Management may include:

• Hearing aids or cochlear implants for hearing loss.
• Surgical correction of digital anomalies if they cause functional impairment.
• Regular monitoring and supportive therapies to address developmental delays and other associated conditions.

Prognosis

The prognosis for individuals with Nasodigitoacoustic syndrome varies depending on the severity of the symptoms. Early intervention and supportive care can improve the quality of life for affected individuals.

Related Pages

• Genetic disorder
• Facial dysmorphism
• Brachydactyly
• Clinodactyly
• Syndactyly
• Sensorineural hearing loss
• Autosomal dominant

See Also

• List of genetic disorders
• Congenital disorder
• Rare disease

External Links

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