Diomedi–Bernardi–Placidi syndrome

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Diomedi–Bernardi–Placidi syndrome is a rare genetic disorder characterized by a combination of symptoms, including intellectual disability, epilepsy, and distinct facial features. The syndrome is inherited in an autosomal recessive manner, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected by the disorder.

Symptoms and Characteristics[edit | edit source]

The primary features of Diomedi–Bernardi–Placidi syndrome include moderate to severe intellectual disability, seizures that are often resistant to treatment, and specific facial dysmorphisms such as a prominent forehead, widely spaced eyes (hypertelorism), a broad nasal bridge, and a thin upper lip. Individuals with this syndrome may also exhibit muscle hypotonia (decreased muscle tone), behavioral problems, and developmental delays.

Genetics[edit | edit source]

Diomedi–Bernardi–Placidi syndrome is caused by mutations in a gene that has not been conclusively identified. The disorder follows an autosomal recessive pattern of inheritance. This means that for a child to be affected, they must receive one mutated gene from each parent. Parents of an affected child are typically unaffected carriers of one copy of the mutated gene.

Diagnosis[edit | edit source]

Diagnosis of Diomedi–Bernardi–Placidi syndrome is based on clinical evaluation and the presence of characteristic symptoms. Genetic testing may confirm the diagnosis by identifying mutations associated with the syndrome, although the specific gene involved may not always be identifiable with current technology.

Management and Treatment[edit | edit source]

There is no cure for Diomedi–Bernardi–Placidi syndrome, and treatment is symptomatic and supportive. Management may include the use of antiepileptic drugs (AEDs) to control seizures, though seizures may be difficult to manage in some cases. Early intervention programs that include physical, occupational, and speech therapy can help improve motor skills and communication abilities. Behavioral therapies may also be beneficial for managing behavioral issues.

Prognosis[edit | edit source]

The prognosis for individuals with Diomedi–Bernardi–Placidi syndrome varies depending on the severity of symptoms and the effectiveness of management strategies. While the syndrome can significantly impact quality of life, appropriate care and support can help improve outcomes.

Diomedi–Bernardi–Placidi syndrome Resources
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Contributors: Prab R. Tumpati, MD