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Adrenoleukodystrophy physical examination

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:

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Overview

Overview

Adrenoleukodystrophy has numerous phenotypes with various clinical findings. The most aggressive one is Childhood cerebral type which results in behavioural changes, school failure, dementia, speech impairment, bulbar palsy, paralysis and audiovisual changes on examination. Most males in childhood have adrenal insufficiency that can show orthostatic hypotension, hyperpigmentation and confusion. Females who are heterozygous and symptomatic can have sphincter disturbances, incoordination and paraparesis.

Physical Examination

Physical Examination

Adrenoleukodystrophy has numerous phenotypes with various clinical findings. Some of the general examination findings which can occur in all phenotypes are listed as following:

HEENT

Neck

Neck examination of patients with Adrenoleukodystrophy is usually normal.

Lungs

Pulmonary examination of patients with Adrenoleukodystrophy is usually normal.

Heart

Cardiovascular examination of patients with Adrenoleukodystrophy is usually normal.

Abdomen

Back

Back examination of patients with Adrenoleukodystrophy is usually normal.

Neuromuscular

Skin

Genitourinary


Physical exam findings related to specific phenotype[1]
Phenotypes Examination Findings
Childhood Cerebral Behavioural changes

Dementia

Speech impairment

Bulbar palsy

Paralysis

Audiovisual disturbances

Adrenomyeloneuropathy (AMN) Paraparesis

Sphincter disturbances

Sensory changes

Incoordination

Addison disease only Orthostatic hypotension

Fever

Weakness

Hyperpigmentation

Seizures

Confusion

Mild myelopathy Increased deep tendon reflexes

Sensory disturbances in lower extremities

Incoordination

Sphincter disturbances

References

References

  1. Moser HW, Raymond GV, Dubey P (2005). “Adrenoleukodystrophy: new approaches to a neurodegenerative disease”. JAMA. 294 (24): 3131–4. doi:10.1001/jama.294.24.3131. PMID 16380594.

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