Living with Alpha-Mannosidosis

At present, there is no cure for the condition, and to date management of Alpha-Mannosidosis has largely focused on treatment of the various symptoms that can be present.1

Some of the main complications include

  • otitis media (inflammation of the ear)
  • hearing loss
  • dental alterations
  • joint problems
  • spinal deformities
  • general orthopedic problems
  • mental retardation1

Each of these problems will have to be cared for by a specialist, in addition to an expert in rare metabolic diseases, and patients are typically seen by an ophthalmologist (eye doctor), an otolaryngologist (ear, nose and throat), hearing specialist and psychiatrist or psychologist, in addition to an orthopedic specialist.1

ophtalmologist

Ophtalmologist

otolaryngologist

Otolaryngologist
Hearing specialist

psychiatric

Psychiatric
or psychologist

orthopedic

Orthopedic
specialist

dentist

Dentist

Ideally, the individual with alpha-mannosidosis will be followed by a team of medical specialists who can help determine the specific needs of each person and help suggest the most appropriate solutions. This may include, for example, the use of a hearing aid, educational interventions to improve social skills and even orthopedic surgery to correct some skeletal abnormalities.1 Whatever interventions are needed, consider that treatment is always proactive, and aimed on preventing complications and treating symptoms of the condition, such as infections.

Today, newer treatments that address the cause of the disease are now being studied.

enzyme replacement therapy

Most recently, in Europe, enzyme replacement therapy has been approved for use in adults, adolescents and children with mild–moderate forms of Alpha-Mannosidosis.2 In enzyme replacement therapy, the defective enzyme is replaced (in this case alpha-mannosidase) with a normal or more active form of the enzyme that is lacking.

bone marrow transplantation (BMT)

Another type of therapy is called bone marrow transplantation (BMT) which may help donor cells repopulate the patient’s tissues and transfer normal enzyme to cells that make the incorrect form.2 However, while considered promising, the procedure may be associated with some risks.2

Thus, while some therapies that have shown encouraging results, your doctor and team of specialists can help determine which treatment is most appropriate after careful assessment and evaluation of the individual with the disease.

  1. Malm, D. & Nilssen, Ø. Alpha-mannosidosis. Orphanet Journal of Rare Diseases 3, 21 (2008).
  2. Ceccarini, M. R. et al. Alpha-Mannosidosis: Therapeutic Strategies. International Journal of Molecular Sciences 19, 1500 (2018).