What is KBG Syndrome

KBG Syndrome is a rare genetic disorder that affects various parts of the body. It is characterized by distinct facial features, intellectual disability, skeletal abnormalities, and developmental delays. The acronym "KBG" stands for the surnames of the three families in which the syndrome was first identified.

Facial features: Individuals with KBG Syndrome often have a prominent forehead, widely spaced eyes, arched eyebrows, a short nose with a broad tip, and a thin upper lip.

Intellectual disability: Most people with KBG Syndrome have some degree of intellectual disability, ranging from mild to moderate.

Skeletal abnormalities: Common skeletal features include short stature, abnormalities in the fingers and toes, and joint problems.

Developmental delays: Children with KBG Syndrome may experience delays in reaching developmental milestones such as walking and talking.

While there is no cure for KBG Syndrome, treatment focuses on managing the symptoms and providing support for individuals and their families. Early intervention programs, educational support, and therapies tailored to the individual's needs can greatly improve their quality of life.