ABCD1
Adrenoleukodystrophy, X-Linked: ABCD1 Sequencing
Key Information
Lab:
TAT:
21 days
Price:
$1,000
CPT Code(s):
81405
Test Code:
DABC
Prenatal Samples Accepted
Adrenoleukodystrophy, X-Linked: ABCD1 Sequencing
ABCD1 sequencing is a molecular test used to identify variants in the gene associated with X-linked Adrenoleukodystrophy. This test can also confirm a diagnosis and identify disease-causing variants within a family to facilitate carrier screening.
X-linked Adrenoleukodystrophy
Clinical Information
X-linked Adrenoleukodystrophy is a neurological disorder characterized by MRI findings in the white matter and adrenal cortex and abnormal plasma concentrations of very long chain fatty acids. The condition can present in three different phenotypes, childhood cerebral form, adrenomyeloneuropathy, and Addison disease only.
The childhood cerebral form has an onset of symptoms between ages 4-8 beginning with ADHD like symptoms with progressive cognitive, behavior, vision, hearing, and motor deterioration. Adrenomyeloneuropathy will usually present in males in their late twenties as sexual dysfunction, progressive paraparesis, sphincter disturbances and abnormalities in adrenocortical function. The mildest presentation is primary adrenocortical insufficiency without significant neurological involvement with onset ranging from two years to adulthood. Some carrier females may experience mild adrenomyeloneuropathy symptoms with a later age of onset.
Technical Information
Specimen Requirements
Transport Instructions
Prenatal Testing Information
Prenatal diagnosis may be available for familial pathogenic or likely pathogenic variants; full sequencing of the ABCD1 gene is not available. For variants identified at external laboratories, GGC will need to review the variant classification prior to sample receipt. Prenatal diagnosis is not available for variants of uncertain clinical significance. Additional fees for cell culture and maternal cell contamination may apply. Maternal cell contamination studies are required for all prenatal molecular tests. Contact the laboratory prior to sending a prenatal specimen to confirm that targeted testing can be accepted.
Prenatal Specimen Requirements
Prenatal Transport Instructions
Connect With Our Experts
Call 1-800-473-9411 to speak with our team of laboratory genetic counselors for questions or additional information.
Robin Fletcher, MS, CGC
Falecia Thomas, MS, CGC
Alex Finley, MS, CGC
