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Adrenoleukodystrophy (ALD) refers to several different inherited conditions that affect the nervous system and adrenal glands. Other names for it are adrenomyeloneuropathy, childhood cerebral ALD, and Schilder-Addison complex.
The gene that causes ALD was identified in 1993. According to the Oncofertility Consortium, it occurs in about 1 in 20,000 to 50,000 people and mainly affects men. Women with the gene tend to be asymptomatic (or mildly symptomatic), meaning there are no symptoms. The symptoms, treatments, and prognosis of ALD vary depending on which type is present. ALD is not curable, but doctors can sometimes slow its progression.
There are three types of ALD:
The adrenoleukodystrophy protein (ALDP) helps your body break down very long chain fatty acids (VLCFA). When this doesn’t happen, the fatty acids build up inside your body. This can harm the outer layer of the cells in your:
People with ALD have mutations in the gene that makes ALDP. Their bodies don’t make enough ALDP.
Men are typically affected by ALD at an earlier age than women and usually have more severe symptoms. ALD affects males more than females because it is X-linked. This means that the gene mutation that causes it is on the X chromosome. Men only have one X chromosome, while women have two copies of it. That means that women can have one normal gene and one copy with the gene mutation.
Women who have only one copy of the mutation have much milder symptoms than men. In some cases, women who carry the gene don’t have symptoms at all. Their normal copy of the gene makes enough ALDP to help mask their symptoms. Most women with ALD have adrenomyelopathy. Addison’s disease and childhood cerebral ALD are less common.
Symptoms of childhood cerebral ALD include:
Signs of adrenomyelopathy include:
Signs of adrenal insufficiency or Addison’s disease include:
ALD symptoms can mimic those of other illnesses. That means that tests are needed to distinguish it from other neurological conditions. Your doctor may order a blood test to:
Your doctor may also look for damage to your brain using an MRI scan. Skin samples or a biopsy and fibroblast cell culture can also be used to test for VLCFAs.
Children with suspected ALD may need additional testing, including vision screens.
Treatment methods depend on the type of ALD you have. Steroids can be used to treat Addison’s disease. There are no specific methods for treating the other types of ALD.
Some people have been helped by:
Doctors continue to look for new ALD treatments. Some are experimenting with bone marrow transplants. If diagnosed early, these procedures may be able to help children with childhood cerebral ALD.
Childhood cerebral ALD can lead to severe disability, coma, and death. Coma typically occurs around two years after symptoms begin appearing and can last for up to 10 years, until death.
Adrenomyelopathy and Addison’s disease are not as serious as childhood cerebral ALD. They progress at a slower rate. The symptoms can be treated, but there is no cure for ALD.
Because ALD is an inherited condition, there’s no way to prevent. If you’re a woman with a family history of ALD, your doctor will recommend genetic counseling before you have children. An amniocentesis or chorionic villus sampling can be done during pregnancy to determine if your unborn child is affected.
Written by: Amanda Delgado and Elizabeth Boskey, PhD
Published on: Jul 16, 2012on: Apr 17, 2017
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