Roberts syndrome

From WikiMD's Wellness Encyclopedia

Virchow fetus 1898

Roberts syndrome is a rare genetic disorder characterized by limb and facial abnormalities. It is also known as pseudothalidomide syndrome due to its phenotypic similarities to the effects of thalidomide exposure. The condition is named after the American geneticist John B. Roberts, who first described it in 1919.

Presentation[edit | edit source]

Individuals with Roberts syndrome typically present with a range of physical abnormalities. These may include:

Genetics[edit | edit source]

Roberts syndrome is inherited in an autosomal recessive manner. The condition is caused by mutations in the ESCO2 gene, which is located on chromosome 8. The ESCO2 gene is responsible for encoding a protein that plays a crucial role in the cohesin complex, which is essential for proper chromosome segregation during cell division.

Diagnosis[edit | edit source]

Diagnosis of Roberts syndrome is based on clinical evaluation and genetic testing. Prenatal diagnosis can be performed through amniocentesis or chorionic villus sampling if there is a known family history of the disorder.

Management[edit | edit source]

There is no cure for Roberts syndrome, and treatment is primarily supportive. Management may include:

  • Surgical correction of limb and craniofacial abnormalities
  • Physical therapy to improve mobility and function
  • Special education programs to address intellectual disabilities

Prognosis[edit | edit source]

The prognosis for individuals with Roberts syndrome varies depending on the severity of the condition. Some individuals may have a relatively normal lifespan with appropriate medical care, while others may experience significant health challenges.

Related Pages[edit | edit source]

See Also[edit | edit source]

References[edit | edit source]

External Links[edit | edit source]

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Contributors: Prab R. Tumpati, MD