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What is Adrenoleukodystrophy?
- Adrenoleukodystrophy: Introduction
- Types of Adrenoleukodystrophy
- Prognosis
- Complications
- Prevalence
- Other names for Adrenoleukodystrophy
- What causes Adrenoleukodystrophy?
- What are the symptoms of Adrenoleukodystrophy?
- Organs Affected by Adrenoleukodystrophy
- Can anyone else get Adrenoleukodystrophy?
- How is it treated?
- Adrenoleukodystrophy: Introduction
What is 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.
- 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: Introduction
Types of 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
- more types...»
Broader types of Adrenoleukodystrophy:
How many people get Adrenoleukodystrophy?
Prevalance of Adrenoleukodystrophy: 1 per 20,000 people suffer from X-linked adrenoleukodystrophy, Genetics Home reference website
Prevalance Rate of Adrenoleukodystrophy: approx 1 in 20,000 or 0.00% or 13,600 people in USA [about data]
How serious is Adrenoleukodystrophy?
Complications of Adrenoleukodystrophy:
see complications of Adrenoleukodystrophy
Prognosis of 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)
What causes Adrenoleukodystrophy?
Causes of Adrenoleukodystrophy: see causes of Adrenoleukodystrophy
What are the symptoms of Adrenoleukodystrophy?
Symptoms of Adrenoleukodystrophy: see symptoms of Adrenoleukodystrophy
Complications of Adrenoleukodystrophy: see complications of Adrenoleukodystrophy
Can anyone else get Adrenoleukodystrophy?
Contagion of genetic conditions:
generally not; see details in contagion of genetic diseases.
Inheritance of genetic conditions: see details in inheritance of genetic diseases.
Adrenoleukodystrophy: Testing
Diagnostic testing: see tests for Adrenoleukodystrophy.
Misdiagnosis: see misdiagnosis and Adrenoleukodystrophy.
How is it treated?
Treatments for Adrenoleukodystrophy:
see treatments for Adrenoleukodystrophy
Research for Adrenoleukodystrophy:
see research for Adrenoleukodystrophy
Organs Affected by Adrenoleukodystrophy:
Organs and body systems related to Adrenoleukodystrophy include:
Name and Aliases of Adrenoleukodystrophy
Main name of condition: Adrenoleukodystrophy
Class of Condition for Adrenoleukodystrophy: genetic
Addison-Schilder disease, ALD, Simerling-Creutzfeldt, Addison-Scholz, Addison-Schilder, bronze syndrome, melanodermic leukodystrophy, sudanophilic leukodystrophy [bronzing of skin - adrenal atrophy], Addison disease [cerebral sclerosis syndrome], addison disease [spastic paraplegia syndrome], Fanconi-Prader syndrome, Siemerling-Creutzfeldt syndrome, adrenocortical atrophy [cerebral sclerosis syndrome], bronze Schilder disease, Addison disease with cerebral sclerosis, encephalitis periaxialis diffusa, Flatau-Schilder disease, Myelinoclastic diffuse sclerosis, X-linked adrenoleukodystrophy, AMN, Adrenomyeloneuropathy, Siemerling-Creutzfeldt disease, Addison disease and cerebral sclerosis
Adrenomyeloneuropathy, Bronze Schilder disease, Siemerling-Creutzfeldt disease, Adrenoleucodystrophy, Addison-Schilder syndrome
Source - Diseases Database
AMN, Addison disease and cerebral sclerosis, Addison-Schilder syndrome, Adrenomyeloneuropathy, Bronze Schilder disease, Schilder's disease, Siemerling-Creutzfeldt disease, Adrenomyeloneuropathy, Bronze Schilder disease, Schilder's disease, Siemerling-Creutzfeldt disease, AMN, Addison disease and cerebral sclerosis, X-linked adrenoleukodystrophy, Adrenoleukodystrophy, X-linked
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)
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