Additional information

Laboratory

Exult Diagnostics, Dr. Lal PathLabs

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Nx GEN SEQUENCING: ADRENOLEUKODYSTROPHY

 20000

EX1603      Nx GEN SEQUENCING: ADRENOLEUKODYSTROPHY
Specimen: Submit 10 mL (5 mL min.) of whole blood from 2 Lavender Top (EDTA) tubes. Ship refrigerated. DO NOT FREEZE.
Stability:
Room Refrigerated Frozen
6 hrs 72 hrs NA
Method: NGS, Sanger sequencing
Comment:
Report: Contact us to know the TAT.
Usage: Mutation in the ABCD1 gene is found to be associated with Adrenoleukodystrophy, also known as X-linked Adrenoleukodystrophy (X-ALD). It is primarily found in males. It is associated with cerebral demyelination, axonal dysfunction in the spinal cord leading to spastic paraplegia, adrenal insufficiency, and in some cases testicular insufficiency. X-ALD is a metabolic disorder characterized by impaired peroxisomal beta-oxidation of very-long-chain fatty acids which is reduced to about 30% of control levels. Consequently, there is an accumulation of VLCFA in the white matter of the brain, spinal cord, and adrenal cortex. The loss of myelin and the progressive dysfunction of the adrenal gland are the primary characteristics of X-ALD. Adrenocortical insufficiency is reported in 70% of all male X-ALD patients prior to the onset of neurological symptoms manifesting with fatigue, nausea, weight loss, hypotension, hypoglycemia, and hypogonadism. X-ALD most severely affects male hemizygotes and less severely affects female heterozygotes. The age of onset and morbidity are highly variable and progression is unpredictable.
Doctor Specialty: Neurologist
Disease: Paralysis
Components: *ABCD1
Courier Charges:
Home Collection: Available (*T&C Apply)
Department: MOLECULAR DIAGNOSTICS
Pre Test Information: A duly filled Whole Exome Sequencing Consent Form is mandatory.