How long does a person live with Treacher Collins syndrome?
A patient diagnosed with Treacher Collins syndrome (TCS) may expect to have approximately the same lifetime as the general population with proper management and a healthy lifestyle. The life expectancy is normal as long as breathing problems during infancy are managed well.
Can Treacher Collins cause death?
In some cases, the prognosis depends on the specific symptoms and severity in the affected person. For example, very severe cases of TCS can cause perinatal death because of a compromised airway.
Can Treacher Collins be cured?
Treacher Collins syndrome is either inherited or caused by a new change in a gene at the time of conception. There is no cure, but skull and face (craniofacial) surgery can improve speech and reduce some of the more severe craniofacial anomalies.
Can Treacher Collins syndrome be prevented?
In most cases, the child’s intelligence is unaffected. Treacher Collins syndrome is either inherited or caused by a new change in a gene at the time of conception. There is no cure, but skull and face (craniofacial) surgery can improve speech and reduce some of the more severe craniofacial anomalies.
Who was the first person to get Treacher Collins syndrome?
TCS occurs in about one in 50,000 people. The syndrome is named after Edward Treacher Collins, an English surgeon and ophthalmologist, who described its essential traits in 1900….
| Treacher Collins syndrome | |
|---|---|
| Causes | Genetic |
| Diagnostic method | Based on symptoms, X-rays, genetic testing |
What is sat syndrome?
The SATB2-associated syndrome (SAS) is a recently described condition, characterized by developmental delay, intellectual disability with absent or limited language skills, palatal and dental abnormalities, behavioral problems, and unusual facial features.
What is Fox syndrome?
Collapse Section. FOXG1 syndrome is a condition characterized by impaired development and structural brain abnormalities. Affected infants are small at birth, and their heads grow more slowly than normal, leading to an unusually small head size (microcephaly ) by early childhood.