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Arthrogryposis is a number of rare, nonprogressive muscle disorders causing stiff joints and abnormal development of muscles. From the Greek word meaning “curved joint,” children with arthrogryposis are born with a limited range of joint motion.

Types of arthrogryposis

Amyoplasia – The most common type of arthrogryposis is an overall lack of muscular development and growth with contracture, a loss of joint motion and deformity of most joints. Babies diagnosed with amyoplasia have dense fibrous tissue and fat instead of skeletal muscle.

Distal arthrogryposis – This type affects only several joints, usually in the hands and feet, and range of motion may be mildly limited.

Classic arthrogryposis – This type usually affects the hands, wrists, elbows, shoulders, hips, feet and knees in varying degrees of severity. The most severe can affect almost every body joint, including the back and jaw. Joint contractures, or loss of joint motion, is frequently accompanied by muscle weakness which contributes to the limited movement.

Syndromic arthrogryposis – This type affects the internal organs, as well as the muscle and joint systems. Internal organ involvement can include breathing problems, feeding problems, possible speech disorders and in some cases, mental retardation.

Some factors that can limit joint movement before birth include:

  • Improperly or incorrectly developed muscles
  • Limited room in the uterus for normal movement
  • Improper formation of the central nervous system and spinal cord
  • Abnormal development of the muscles, tendons, bones or joints
  • Genetic, the condition is passed from parent to child

Signs of arthrogryposis

The specific joint contractures in infants vary, but there are several common characteristics that include:

  • A child’s arms and legs are affected, with the most deformity in the wrists and ankles
  • Arm and leg joints may not be able to move
  • Arm and leg muscles are thin and sometimes absent
  • A newborn’s hips may be dislocated

Some infants diagnosed with arthrogryposis may have facial deformities, curvature of the spine, genital deformities, cardiac and respiratory problems and skin defects.

Diagnosing arthrogryposis

There are several ways to diagnose arthrogryposis:

Blood tests – A simple blood test can detect if a newborn has arthrogryposis.

X-rays – In many cases, X-rays are taken to confirm an arthrogryposis diagnosis and to evaluate stiff or dislocated joints.

Muscle biopsies – Another method to diagnose arthrogryposis is to take a muscle sample where any joint deformity can be detected.

Evaluation and treatment of arthrogryposis

For most types of arthrogryposis, a rigorous treatment of physical and occupational therapy can be successful in the improvement of the range of motion of the affected joints. In addition, patients may need:

Splints – Splints are made to increase the stretching exercises and increase the range of motion. Casting is frequently done to improve foot position. Removable splints can be used on knees and feet to allow exercises, but some patients experience significant results by wearing splints at night.

Surgery – Some children may require surgery to address any deformities that the child may have been born with and can include elbows, feet, hips, knees and wrists. Surgery is generally recommended if more range of motion is needed after therapy has achieved maximum results.

Why choose us?

Arthrogryposis multiplex congenita clinic

The Greenville Shriners Hospital provides world-class expertise in the evaluation and treatment of children with AMC. A multidisciplinary team of neurologists, geneticists, physical and occupational therapists, and pediatric orthopaedic surgeons work together to achieve non-operative and operative management of the condition. The goals of management include improving range of motion, achieving ambulation and promoting independence in life’s daily activities. The upper and lower extremity teams work in concert to achieve these goals and coordinate care to maximize the child’s potential.

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