What Is Klumpke’s Palsy? Causes, Symptoms, and Treatment

Klumpke’s Palsy is a specific type of nerve damage affecting the arm and hand, medically known as a lower brachial plexus injury. This injury involves the network of nerves that transmits signals from the spinal cord, controlling movement and sensation in the arm. It most frequently occurs in newborns due to trauma during the birthing process, but it can also result from traumatic injuries in adults. Klumpke’s Palsy is characterized by weakness or paralysis in the muscles of the forearm and hand.

Understanding the Nerve Roots Involved

The brachial plexus originates from the spinal cord (C5 to T1) and is responsible for all motor and sensory function in the shoulder, arm, and hand. Klumpke’s Palsy is defined as an injury to the lower part of this network, primarily involving the C8 and T1 nerve roots.

The injury typically results from excessive upward stretching of the arm, known as hyperabduction. This often occurs during a difficult vaginal delivery, such as when the baby’s shoulder gets lodged (shoulder dystocia) or during a breech presentation. This mechanism causes damage ranging from a mild stretch to a complete tear from the spinal cord.

This lower plexus injury distinguishes Klumpke’s Palsy from Erb’s Palsy, which involves the upper nerve roots (C5 and C6) and affects the shoulder and elbow. Damage to the C8 and T1 roots disrupts signals to the muscles controlling the wrist and hand. The degree of nerve damage dictates the severity of symptoms; a mild stretch (neuropraxia) offers the best chance for full recovery.

Key Signs and Symptoms of Klumpke’s Palsy

The physical effects of Klumpke’s Palsy are concentrated in the forearm, wrist, and hand. The most characteristic presentation is a loss of movement and sensation along the inner side of the arm and hand (C8 and T1 dermatomes). A hallmark sign is the development of a “claw hand,” a deformity caused by the paralysis of the small, intrinsic muscles within the hand.

The intrinsic hand muscles, controlled by the C8 and T1 nerves, are responsible for fine motor movements like flexing and spreading the fingers. When these muscles are paralyzed, opposing forearm muscles pull the fingers into an unnatural position. This results in the wrist and fingers being flexed, giving the hand a claw-like appearance.

In cases where the T1 nerve root is severely affected, the injury may also involve the nearby sympathetic nerve chain. Damage to this chain can result in Horner’s syndrome on the same side of the body. Signs of Horner’s syndrome include a drooping eyelid (ptosis) and an abnormally constricted pupil (miosis).

Diagnosing the Condition and Initial Treatment

Diagnosis begins with a physical examination where a doctor assesses the infant’s reflexes, muscle strength, and ability to move the affected arm and hand. Observing a limp arm, hand weakness, and the characteristic claw hand posture are key indicators. Imaging tests are often used to rule out related issues, such as fractures or dislocations of the shoulder or collarbone.

To pinpoint the location and severity of the nerve damage, doctors use Electromyography (EMG) and Nerve Conduction Studies (NCS). NCS measures the speed and strength of electrical signals through the nerve, while EMG assesses muscle electrical activity. These tests determine if the injury is a mild stretch or a more severe tear, guiding the initial treatment plan.

Initial treatment is typically non-surgical, focusing on supportive care while the nerves heal. The arm may be gently immobilized briefly to protect the injured nerves. This is quickly followed by the introduction of gentle physical and occupational therapy.

Therapy involves passive range-of-motion exercises performed by caregivers several times daily. The purpose of these exercises is to maintain joint flexibility, prevent muscle shortening (contractures), and avoid muscle atrophy while the nerve regenerates. Maintaining joint health ensures the limb is functional when nerve signals eventually return.

Prognosis and Rehabilitation

The recovery outlook for Klumpke’s Palsy is favorable, especially for common cases involving a mild stretching of the nerve fibers (neuropraxia). The majority of infants with neuropraxia regain full or near-full function of their arm and hand. Spontaneous recovery often occurs within the first few months, with many cases resolving completely within six to twelve months after birth.

Long-term rehabilitation involves continuous monitoring and physical therapy to encourage muscle use and improve coordination. This ongoing therapy prevents residual weakness or stiffness from causing lasting functional limitations. Therapists work to integrate the affected arm into daily activities, promoting natural movement patterns.

In severe cases, such as a complete tear (avulsion) or rupture, where no functional improvement is seen after three to six months, surgical intervention may be considered. Options include nerve grafting (using a healthy nerve segment to bridge the gap) or nerve transfer (rerouting a less-essential nerve to power a paralyzed muscle). Although surgery can help restore function, the recovery process is long, and some permanent weakness may remain.