Urban–Rogers–Meyer syndrome

Autosomal recessive - en

Urban–Rogers–Meyer syndrome is a rare genetic disorder characterized by a combination of distinctive craniofacial features, skeletal abnormalities, and developmental delay. The syndrome is named after the researchers who first described it.

Presentation

Individuals with Urban–Rogers–Meyer syndrome typically present with a range of symptoms that can vary in severity. Common features include:

• Craniofacial dysmorphisms: These may include a prominent forehead, wide-set eyes (hypertelorism), a broad nasal bridge, and a small jaw (micrognathia).
• Skeletal abnormalities: These can include short stature, scoliosis, and abnormalities in the bones of the hands and feet.
• Developmental delay: Affected individuals often experience delays in reaching developmental milestones, such as walking and talking. Intellectual disability may also be present.

Genetics

Urban–Rogers–Meyer syndrome is believed to be inherited in an autosomal recessive manner. This means that an individual must inherit two copies of the mutated gene, one from each parent, to be affected by the disorder. The specific gene or genes involved in Urban–Rogers–Meyer syndrome have not yet been identified.

Diagnosis

Diagnosis of Urban–Rogers–Meyer syndrome is typically based on clinical evaluation and the presence of characteristic features. Genetic testing may be used to confirm the diagnosis and to distinguish it from other similar syndromes.

Management

There is no cure for Urban–Rogers–Meyer syndrome, and treatment is primarily supportive and symptomatic. Management may involve a multidisciplinary team, including:

• Pediatricians and geneticists for overall care and genetic counseling.
• Orthopedic surgeons for skeletal abnormalities.
• Speech therapists and occupational therapists for developmental support.

Prognosis

The prognosis for individuals with Urban–Rogers–Meyer syndrome varies depending on the severity of symptoms. With appropriate medical care and support, many individuals can lead fulfilling lives.

See also

• Genetic disorder
• Craniofacial dysmorphisms
• Developmental delay
• Autosomal recessive

Related pages

• Genetic testing
• Intellectual disability
• Scoliosis
• Micrognathia