DOPEY2

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Dopey2: A Comprehensive Guide to the Rare Genetic Disorder

Description

Dopey2 is an extremely rare genetic disorder caused by mutations in the TBL1XR1 gene. It is characterized by a distinctive facial appearance, which includes a rounded face, short stature, and microcephaly (small head circumference). Other common features of Dopey2 include intellectual disability, speech and language delays, and behavioral problems.

Associated Diseases

Dopey2 is not known to be associated with any specific diseases. However, individuals with Dopey2 may be at an increased risk for certain health conditions, such as:

• Autism spectrum disorder (ASD)
• Attention deficit hyperactivity disorder (ADHD)
• Obesity
• Seizures

Did you Know ?

Dopey2 is an extremely rare disorder, with an estimated prevalence of less than one in a million live births.