Craniosynostosis, Philadelphia type

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Obesity, Sleep & Internal medicine
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Craniosynostosis, Philadelphia type
Synonyms	Philadelphia type craniosynostosis
Pronounce	N/A
Specialty	N/A
Symptoms	Premature closure of cranial sutures, abnormal skull shape
Complications	Increased intracranial pressure, developmental delay
Onset	Infancy
Duration	Lifelong
Types	N/A
Causes	Genetic mutation
Risks	Family history
Diagnosis	Clinical examination, genetic testing
Differential diagnosis	Other types of craniosynostosis
Prevention	N/A
Treatment	Surgical intervention
Medication	None specific
Prognosis	Variable, depends on severity and treatment
Frequency	Rare
Deaths	Rarely directly causes death

A rare genetic disorder affecting skull development

Craniosynostosis, Philadelphia type is a rare genetic disorder characterized by the premature fusion of certain bones in the skull, leading to an abnormal head shape and potentially affecting brain development. This condition is a form of craniosynostosis, which refers to the early closure of one or more of the cranial sutures, the fibrous joints between the bones of the skull.

Genetics

Craniosynostosis, Philadelphia type, is inherited in an autosomal dominant pattern, meaning that a single copy of the altered gene in each cell is sufficient to cause the disorder. The specific genetic mutation responsible for this condition has been identified in the EFNB1 gene, which plays a crucial role in the development of the cranial sutures.

Autosomal dominant inheritance pattern

Clinical Features

Individuals with Craniosynostosis, Philadelphia type, typically present with a distinct set of craniofacial abnormalities. These may include:

• Brachycephaly: A short and broad head shape due to the premature fusion of the coronal sutures.
• Hypertelorism: An increased distance between the eyes.
• Midface hypoplasia: Underdevelopment of the middle facial region.
• Proptosis: Protrusion of the eyes due to shallow eye sockets.

In addition to these craniofacial features, affected individuals may experience developmental delays and intellectual disabilities, although the severity can vary widely among patients.

Diagnosis

The diagnosis of Craniosynostosis, Philadelphia type, is typically made based on clinical examination and imaging studies. Computed tomography (CT) scans of the skull can reveal the premature fusion of the cranial sutures. Genetic testing can confirm the presence of mutations in the EFNB1 gene, supporting the diagnosis.

Management

Management of Craniosynostosis, Philadelphia type, often involves a multidisciplinary approach. Surgical intervention may be necessary to correct the cranial deformities and prevent complications such as increased intracranial pressure. Cranial vault remodeling is a common surgical procedure used to reshape the skull and allow for normal brain growth. In addition to surgical treatment, supportive therapies such as speech therapy, occupational therapy, and physical therapy may be beneficial in addressing developmental delays and improving quality of life.

Prognosis

The prognosis for individuals with Craniosynostosis, Philadelphia type, varies depending on the severity of the condition and the presence of associated complications. Early diagnosis and appropriate management can significantly improve outcomes and help individuals lead fulfilling lives.

See also

• Craniosynostosis
• Genetic disorder
• Autosomal dominant
• Cranial sutures