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Adrenoleukodystrophy
Introduction: Adrenoleukodystrophy
Adrenoleukodystrophy: Adrenoleukodystrophy (ALD) is a rare, inherited metabolic disorder that afflicts the young boy Lorenzo Odone, whose story is told in the 1993 film "Lorenzo's oil." In ... more about Adrenoleukodystrophy.
Adrenoleukodystrophy: A rare disorder which has characteristic symptoms of Addison disease (adrenocortical insufficiency) and Schilder disease (cerebral sclerosis). Bronze skin, brain sclerosis and demyelination are the main symptoms. More detailed information about the symptoms, causes, and treatments of Adrenoleukodystrophy is available below.
Symptoms of Adrenoleukodystrophy
- Seizures
- Impaired motor function
- Impaired vision
- Swallowing difficulties
- Attention problems
See full list of 46 symptoms of Adrenoleukodystrophy
Home Diagnostic Testing
Home medical testing related to Adrenoleukodystrophy:
- Fatigue: Related Home Tests:
- Adrenal Gland Health: Home Testing:
Medical Textbooks Online about Adrenoleukodystrophy
Free access (no registration).
- "Professional Guide to Signs & Symptoms (Fifth Edition)"
- [ read ]
Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.
Causes of Adrenoleukodystrophy
Read more about causes of Adrenoleukodystrophy.
Videos for Adrenoleukodystrophy
Taking Part in CML Trials
Hear one woman's story as she participates in a clinical trial to help fight CML.
Monitoring CML
A wide range of laboratory tests is used to monitor a patient's response to therapy for chronic myeloid leukemia. Listen to experts explain the...
Responses to CML Treatments
One of the greatest success stories in cancer treatment occurs in people with chronic myeloid leukemia. But treatments don't always work well in...
Emerging Therapies for CML
A majority of people with CML do well with treatments. But a few will develop serious side effects or develop drug resistance. Listen to experts...
Patient Surveys for Adrenoleukodystrophy
- Patient Profile Survey
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Prognosis for Adrenoleukodystrophy
Prognosis for Adrenoleukodystrophy: Prognosis for patients with ALD is generally poor except after successful bone marrow transplantation. Death may occur within 1 to 10 years after the onset of symptoms due to disease progression. (Source: excerpt from NINDS Adrenoleukodystrophy Information Page: NINDS)
More about prognosis of Adrenoleukodystrophy
Reseach about Adrenoleukodystrophy
Visit our research pages for current research about Adrenoleukodystrophy treatments.
Clinical Trials for Adrenoleukodystrophy
The US based website ClinicalTrials.gov lists information on both federally and privately supported clinical trials using human volunteers.
Some of the clinical trials listed on ClinicalTrials.gov for Adrenoleukodystrophy include:
- Study of Glyceryl Trierucate and Glyceryl Trioleate (Lorenzo's Oil) Therapy in Male Children With Adrenoleukodystrophy - This study is currently recruiting patients (Current: 23 Nov 2006) - glyceryl trierucate,glyceryl trioleate
- Study of Bile Acids in Patients With Peroxisomal Disorders - This study is not yet open for patient recruitment (Current: 23 Nov 2006) - chenodeoxycholic acid,cholic acid,ursodiol
- Randomized Study of Beta Interferon and Thalidomide in Patients With Adrenoleukodystrophy - This study has been completed (Current: 23 Nov 2006) - glyceryl trierucate,glyceryl trioleate,interferon beta,thalidomide
- Study of Pulmonary Complications in Pediatric Patients With Storage Disorders Undergoing Allogeneic Hematopoietic Stem Cell Transplantation - This study is no longer recruiting patients (Current: 23 Nov 2006)
- Study of Oral Cholic Acid in Patients With Inborn Errors of Bile Acid Synthesis - This study has been completed (Current: 23 Nov 2006)
See full list of 9 Clinical Trials for Adrenoleukodystrophy
Statistics for Adrenoleukodystrophy
- Medical statistics for Adrenoleukodystrophy
- Prevalence and incidence statistics for Adrenoleukodystrophy
- Death and Mortality statistics for Adrenoleukodystrophy
- Society statistics for Adrenoleukodystrophy
Types of Adrenoleukodystrophy
- Classic childhood ALD - severe form in boys
- Adult-onset ALD - milder form in young adults
- Female carrier ALD - mild form in female carrying the gene.
- Neonatal ALD
Read more about Types of Adrenoleukodystrophy
Medical Guidebooks and Ebooks for Adrenoleukodystrophy
See all guides and ebooks for Adrenoleukodystrophy
Stories from Users Related to Adrenoleukodystrophy
- Adrenal dysfunction?
- So many untreated symptoms... enlarged liver, cerebral atrophy, acid reflux, etc.
- bronze skin.
- cerebral atrophy
- Leukodystrophy
- please help my mum! Paraplegia
- X-linked agamglobulinemia
- Is it Addison's Disease?
- x-ray help
- addisons disease
- spastic legs
- Severe adrenal rushes
- paraplegia....
- could this be Spastic pelvic floor syndrome?
- atrophy in cerebellum
- Diffused Disc
- Arm atrophy
- Rounded shadows & "wispy" x-ray images around my lower tibia
- Right arm atrophy
- Depo Provera Shot... Please help, I'm at my wits end x
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Article Excerpts about Adrenoleukodystrophy
Genes and Disease by the National Center for Biotechnology (Excerpt)
Adrenoleukodystrophy (ALD) is a rare, inherited metabolic disorder that afflicts the young boy Lorenzo Odone, whose story is told in the 1993 film "Lorenzo's oil." In this disease, the fatty covering (myelin sheath) on nerve fibers in the brain is lost, and the adrenal gland degenerates, leading to progressive neurological disability and death. (Source: Genes and Disease by the National Center for Biotechnology)
NINDS Adrenoleukodystrophy Information Page: NINDS (Excerpt)
Adrenoleukodystrophy (ALD) is a rare, genetic disorder characterized by the breakdown or loss of the myelin sheath surrounding nerve cells in the brain and progressive dysfunction of the adrenal gland. ALD is one of a group of genetic disorders called the leukodystrophies that cause damage to the myelin sheath, the fatty covering — which acts as an insulator — on nerve fibers in the brain. (Source: excerpt from NINDS Adrenoleukodystrophy Information Page: NINDS)
Definitions of Adrenoleukodystrophy:
A syndrome combining the characteristics of adrenocortical insufficiency (Addison disease) with those of cerebral sclerosis (Schilder disease). Skin bronzing and sclerosis of the brain and demyelination are the principal manifestations. - (Source - Diseases Database)
Adrenoleukodystrophy is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Adrenoleukodystrophy, or a subtype of Adrenoleukodystrophy,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
- Adrenoleukodystrophy
- What is Adrenoleukodystrophy?
- Online Medical Textbooks for Adrenoleukodystrophy
- Prevalence and Incidence of Adrenoleukodystrophy
- Videos related to Adrenoleukodystrophy
- Prognosis of Adrenoleukodystrophy
- Types of Adrenoleukodystrophy
- Causes of Adrenoleukodystrophy
- Causes in Children
- Information Guides
- Symptoms of Adrenoleukodystrophy
- Diagnostic Tests for Adrenoleukodystrophy
- Diagnosis of Adrenoleukodystrophy
- Signs of Adrenoleukodystrophy
- Complications of Adrenoleukodystrophy
- Treatments for Adrenoleukodystrophy
- Doctors and Medical Specialists for Adrenoleukodystrophy
- Cure Research for Adrenoleukodystrophy
- Statistics about Adrenoleukodystrophy
- Statistics by Country for Adrenoleukodystrophy
- Articles about Adrenoleukodystrophy
- Glossary for Adrenoleukodystrophy
- Clinical Trials for Adrenoleukodystrophy
- External links relating to Adrenoleukodystrophy
- SPASTICITY (Algorithmic Diagnosis of Symptoms and Signs)
- Paraplegia (In a Page: Signs and Symptoms)
- Gait, spastic [Hemiplegic gait] (Handbook of Signs & Symptoms (Third Edition))
- Muscle spasticity [Muscle hypertonicity] (Handbook of Signs & Symptoms (Third Edition))
- Adrenal Insufficiency (A Pocket Manual of Differential Diagnosis)
- Peripheral Neuropathy (A Pocket Manual of Differential Diagnosis)
- Adrenal crisis (Professional Guide to Diseases (Eighth Edition))
- Adrenal hypofunction (Professional Guide to Diseases (Eighth Edition))
- Creutzfeldt-Jakob disease (Professional Guide to Diseases (Eighth Edition))
- Encephalitis (Professional Guide to Diseases (Eighth Edition))
- West Nile encephalitis (Professional Guide to Diseases (Eighth Edition))
- Skin, bronze (Professional Guide to Signs & Symptoms (Fifth Edition))
- Gait, spastic [Hemiplegic gait] (Professional Guide to Signs & Symptoms (Fifth Edition))
- Muscle spasticity [Muscle hypertonicity] (Professional Guide to Signs & Symptoms (Fifth Edition))
- Peripheral Neuropathy (Field Guide to Bedside Diagnosis)
- Adrenal hypofunction (Handbook of Diseases)
- Creutzfeldt-Jakob disease (Handbook of Diseases)
- Encephalitis (Handbook of Diseases)
- West Nile encephalitis (Handbook of Diseases)
- Skin, bronze (Signs & Symptoms: A 2-in-1 Reference for Nurses)
- Muscle spasticity (Signs & Symptoms: A 2-in-1 Reference for Nurses)
- Gait, spastic [Hemiplegic gait] (Nursing: Interpreting Signs and Symptoms)
- Muscle spasticity [Muscle hypertonicity] (Nursing: Interpreting Signs and Symptoms)
» Next page: What is Adrenoleukodystrophy?
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- What is Adrenoleukodystrophy?
- Online Medical Textbooks for Adrenoleukodystrophy
- Prevalence and Incidence of Adrenoleukodystrophy
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- Prognosis of Adrenoleukodystrophy
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