Arthrogryposis Multiplex Congenita

Original Editors - Casey Sisk and Shelby White

Top Contributors - Casey Sisk, Jess Bell, Kim Jackson, Robin Tacchetti, Uchechukwu Chukwuemeka, Mande Jooste, Evan Thomas, Shelby White, Rucha Gadgil, 127.0.0.1, WikiSysop, Meaghan Rieke, Nupur Smit Shah, Elaine Lonnemann, Naomi O'Reilly, George Prudden and Priyanka Chugh

Introduction

Arthrogryposis Multiplex Congenita (AMC) "describes joint contractures in two or more areas of the body." AMC is not a specific diagnosis. Contractures can be caused by a range of medical conditions. If a congenital contracture forms in just one area, it is not considered AMC. Instead it is referred to as an isolated congenital contracture (e.g. clubfoot). AMC is a non-progressive condition of unknown cause that is diagnosed at birth.

Prevalence

AMC occurs in around 1 in 3,000 live births. It affects males and females almost equally and it occurs in Asian, African and European populations.

Characteristics/Clinical Presentation

The signs and symptoms of AMC vary considerably from person to person. There are over 400 conditions and syndromes that come under the umbrella of AMC, so the following categories have been proposed:

• Amyoplasia
• Distal
• Other types of arthrogryposis

The prognosis of AMC depends on the underlying cause of the condition in each individual, as well as the extent of contractures and other changes associated with the condition. It is estimated that around one-third of infants born with AMC are stillborn or die before their first birthday.

For more information on AMC, please see the AMSCI website.

Clinical signs and symptoms of AMC include:

• Decreased or absent movement around small and large joints due to contractures
• Muscles of affected limbs are underdeveloped with decreased strength and bulk
• Long bones of the arms and legs are fragile
• Slender build
• Cleft palate
• Cognition may or may not be affected
• Around one-third of babies affected have structural or functional abnormalities of the central nervous system (CNS)
• Usually painless to the child

The most typical presentations of AMC are:

1. Flexed and dislocated hips, extended knees, clubfeet, internally rotated shoulders, flexed elbows, and flexed and ulnarly deviated wrists
2. Abducted and externally rotated hips, flexed knees, clubfeet, internally rotated shoulder, extended elbows, and flexed and ulnarly deviated wrists

Depending on the type of AMC, individuals may also present with:

• Neurologic conditions including epilepsy, defects in neural migration, cerebral hypoplasia, holoprosencephaly, pyramidal tract degeneration, and olivopontocerebellar degeneration
• Congenital heart defect
• Respiratory problems

Aetiology

The aetiology of AMC is unknown, but it is believed that this condition begins in the first trimester of pregnancy. There are several theories on the cause of AMC, including:

• Decreased movement in utero allowing excessive connective tissue to form around the joints (i.e. fibrous ankylosis). This can cause the joint to become fixed / limit joint movement. Decreased foetal movement can have various causes, including foetal crowding (e.g. in multiple births), maternal disorders (viral infections, drug use, trauma, or other maternal illness), and low levels of amniotic fluid around the foetus.
• Genetic and environmental factors

• Chromosomal disorders
• Connective tissue disorders

• Less commonly, AMC can be associated with specific muscle conditions, including muscular dystrophy, some mitochondrial disorders, and congenital myopathies

Differential Diagnosis

Because AMC is an umbrella term, the differential diagnosis covers many conditions and symdromes. Conditions that might be considered in a differential diagnosis, include:

• bony fusion (symphalangism, coalition, synostosis)
• contractural arachnodactyly (Beals syndrome)
• multiple pterygium syndrome
• lethal multiple pterygium syndrome
• osteochondrodysplasias
• distal arthrogryposis
• Freeman-Sheldon syndrome

Diagnostic Tests

The diagnosis of AMC relies heavily on the clinical examination and evaluation of characteristic symptoms and a detailed patient history. However, other tests that may be done include:

• Ultrasound- used to diagnose lack of foetal mobility and abnormal position in the womb
• Nerve conduction, electromyography and muscle biopsy - to diagnose myopathic or neuropathic disorder
• Imaging studies of the central nervous system (CNS)
• Comparative genomic hybridization (CGH) array - used to identify segmental DNA copy number changes
• Microarray
• Exome studies

Rehabilitation Management

There is no specific cure for AMC, but it can be managed with surgical and conservative treatment approaches.

Rehabilitation (occupational therapy, physiotherapy etc) are first-line treatments for AMC. The goal of rehabilitation is to maintain and maximise function, improve joint range of motion and prevent further muscle atrophy. Based on current evidence, physiotherapy treatments for AMC might include:

• Gentle joint manipulation
• Use of removable splints for the knees and feet that enable movement
• Night splints are often used from around 1.5 years until age 10, and braces for as long as needed
• Application of appropriate orthotics to assist mobility and enhance independence
• Serial casting of contracted joints
• Standing programmes
• Muscle strengthening, specifically the hip extensors, quadriceps, and shoulder depressors
• Stretching of joint and muscle contractures to promote active movement and avoid immobilisation
• Establishing a home stretching programme with family / caregivers (3-5 times a day, 3-5 repetitions per set, holding each stretch 20-30 seconds)
• Aquatic therapy
• Hippotherapy
• Prescribing assistive devices (e.g. gait trainer, a walker, crutches, etc)
• Dynamic trunk strengthening
• Ambulation either independently or with an assistive device
• Physiotherapy specifically for infants might include: gross motor skills (rolling, sitting, crawling, standing, walking, etc), foot abduction braces, thermoplastic serial splinting, position activities such as stretching the hip flexors and prone positioning, and standing in a standing frame/stander.

Surgical Management

Surgical options might be considered if joint contractures persist after other rehabilitation approaches have been tried. Surgical options vary depending on the location of the contractions.

Surgical interventions may include osteotomies and tendon/ muscle lengthening. In AMC, the tissues surrounding the contracted joint are also affected, which can add complexity to treatment. If an individual with AMC does have muscular limitations, tendon transfers may be performed to improve the length tension relationship and the mechanics of the specific muscle. If a tendon is causing a joint to be held in an abnormal position, a tenotomy can be performed to release the joint from the pull of the tendon. These procedures are usually assisted by capsulotomies as well.

If surgery is being discussed as an option for the child, the following factors are relevant to consider:

• Soft tissue surgery, such as tendon transfers, should be done early in life (ages 3-12 months)
• Other procedures, such as opponensplasty or osteotomies, should be performed later in life when the joint is almost finished growing
• Casting and bracing are often applied post-operatively