oligomelia

the infant was diagnosed with severe oligomelia in all four limbs.

oligomelia can be a sign of underlying genetic disorders.

prenatal ultrasound revealed the presence of oligomelia in the fetus.

further investigation was needed to determine the cause of the oligomelia.

surgical intervention may be considered to improve function in cases of oligomelia.

the patient's medical history included a previous diagnosis of oligomelia.

oligomelia is a rare congenital condition characterized by shortened limbs.

genetic testing was performed to rule out syndromes associated with oligomelia.

the severity of oligomelia varied significantly among the affected individuals.

physical therapy is often recommended for children with oligomelia.

the radiographic findings confirmed the presence of oligomelia in the patient.