Adrenoleukodystrophy
Alternate Names : Melanodermic Leukodystrophy, NALD, Neonatal Adrenoleukodyrstophy, X-Linked Adrenoleukodystrophy
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Prevention
Genetic counseling is recommended for prospective parents with a family history of adrenoleukodystrophy. The carrier state in females can be diagnosed in 85% of the cases using a very long fatty acid assay and a DNA probe study by specialized laboratories. Intrauterine diagnosis of adrenoleukodystrophy is available and done by evaluation of cells from chorionic villus sampling or from amniotic cells (amniocentesis).
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