Radial aplasia

From WikiMD's Wellness Encyclopedia

Radial aplasia (also known as radial club hand) is a rare congenital condition characterized by the underdevelopment or absence of the radius bone in the forearm. This condition can occur in one or both arms and can vary in severity.

Causes[edit | edit source]

The exact cause of radial aplasia is unknown, but it is believed to be due to a disruption in the normal development of the arm during the early stages of pregnancy. Some cases have been associated with certain genetic conditions, such as Fanconi anemia and Holt-Oram syndrome, but in many cases, the cause is unknown.

Symptoms[edit | edit source]

The main symptom of radial aplasia is the underdevelopment or absence of the radius bone. This can result in a variety of physical abnormalities, including a shortened forearm, a hand that is bent towards the thumb side of the arm (radial deviation), and underdeveloped or absent thumbs. Other symptoms can include limited mobility in the affected arm and hand, and in severe cases, other skeletal abnormalities may be present.

Diagnosis[edit | edit source]

Radial aplasia is usually diagnosed at birth based on the physical appearance of the arm and hand. Imaging tests, such as X-rays, can confirm the diagnosis and determine the extent of the condition. Genetic testing may also be performed to identify any associated genetic conditions.

Treatment[edit | edit source]

Treatment for radial aplasia depends on the severity of the condition and the specific symptoms present. Treatment options can include physical therapy, splinting or casting, and in some cases, surgery. The goal of treatment is to improve function and appearance of the arm and hand.

Prognosis[edit | edit source]

The prognosis for individuals with radial aplasia varies depending on the severity of the condition and the presence of any associated conditions. With appropriate treatment, many individuals with radial aplasia can lead normal, healthy lives.

See also[edit | edit source]

Radial aplasia Resources
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Contributors: Prab R. Tumpati, MD