Acropectoral syndrome

Acropectoral syndrome
Synonyms
Pronounce
Specialty	Medical genetics
Symptoms	Limb malformations, pectoral defects
Complications	N/A
Onset
Duration
Types
Causes	Genetic mutation
Risks
Diagnosis	Clinical examination, genetic testing
Differential diagnosis
Prevention
Treatment	Surgical intervention, physical therapy
Medication
Prognosis
Frequency
Deaths

This template provides a structured format for presenting key information about the medical condition known as Acropectoral syndrome. It includes sections for the name, image, specialty, symptoms, causes, diagnosis, and treatment, among others. The use of internal links allows for easy navigation to related topics within a MediaWiki environment. == Acropectoral Syndrome ==

Diagram illustrating autosomal dominant inheritance.

Acropectoral syndrome is a rare genetic disorder characterized by the combination of limb and chest wall abnormalities. It 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.

Clinical Features

Individuals with acropectoral syndrome typically present with a range of physical anomalies. These may include:

• Limb Abnormalities: Affected individuals often have malformations of the hands and feet, such as syndactyly (fusion of fingers or toes), polydactyly (extra fingers or toes), or brachydactyly (short fingers or toes).
• Chest Wall Abnormalities: The syndrome is also associated with defects in the chest wall, such as pectus excavatum (sunken chest) or pectus carinatum (protruding chest).

Genetic Basis

Acropectoral syndrome is caused by mutations in specific genes that are involved in the development of the limbs and chest wall. The exact genetic mutations can vary among affected individuals, but they all follow an autosomal dominant inheritance pattern. This means that if one parent has the syndrome, there is a 50% chance of passing the condition to their offspring.

Diagnosis

Diagnosis of acropectoral syndrome is primarily based on clinical evaluation and the identification of characteristic physical features. Genetic testing can confirm the diagnosis by identifying mutations in the relevant genes.

Management

Management of acropectoral syndrome is typically supportive and symptomatic. Treatment may involve:

• Surgical Interventions: Corrective surgery may be necessary to address significant limb or chest wall deformities.
• Physical Therapy: To improve mobility and function of the affected limbs.
• Genetic Counseling: For affected individuals and their families to understand the inheritance pattern and risks for future offspring.

Related Pages

• Syndactyly
• Polydactyly
• Pectus excavatum
• Pectus carinatum
• Autosomal dominant