Acropectoral syndrome: Difference between revisions
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[[File:Autosomal dominant - en.svg|thumb|right|Diagram illustrating autosomal dominant inheritance.]] | [[File:Autosomal dominant - en.svg|thumb|right|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. | '''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. | ||
Latest revision as of 06:05, 27 April 2025
| Acropectoral syndrome | |
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| 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 | |
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[edit]
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[edit]
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[edit]
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[edit]
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[edit]
| Genetic disorders relating to deficiencies of transcription factor or coregulators | ||||||||||||||||||||||||||||||||||
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