Dahlberg Borer Newcomer syndrome
Dahlberg Borer Newcomer syndrome (pronunciation: Dahl-berg Bor-er New-comer syn-drome) is a rare genetic disorder characterized by skeletal abnormalities, growth retardation, and distinctive facial features.
Etymology
The syndrome is named after the three researchers, Dahlberg, Borer, and Newcomer, who first described the condition in the medical literature.
Symptoms
The symptoms of Dahlberg Borer Newcomer syndrome include short stature, microcephaly (small head size), micrognathia (small jaw), hypertelorism (wide-set eyes), and brachydactyly (short fingers and toes). Other features may include intellectual disability and delayed development.
Causes
Dahlberg Borer Newcomer syndrome is a genetic disorder, which means it is caused by changes (mutations) in genes. The specific gene associated with this condition is not yet known.
Diagnosis
Diagnosis of Dahlberg Borer Newcomer syndrome is based on the presence of characteristic clinical features. Genetic testing may be used to confirm the diagnosis.
Treatment
Treatment of Dahlberg Borer Newcomer syndrome is symptomatic and supportive, focusing on managing the individual symptoms and complications. This may include physical therapy for motor delays, special education for learning difficulties, and surgery for skeletal abnormalities.
Prognosis
The prognosis for individuals with Dahlberg Borer Newcomer syndrome varies depending on the severity of symptoms. With appropriate management and care, individuals with this condition can lead a normal life.
See also
External links
- Medical encyclopedia article on Dahlberg Borer Newcomer syndrome
- Wikipedia's article - Dahlberg Borer Newcomer syndrome
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