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Leucodistrofia de las células globoides; Deficiencia de galactosilcerebrosidasa; Deficiencia de galactosilceramidasa
Se recomienda la asesoría genética para los futuros padres con antecedentes familiares de la enfermedad de Krabbe que estén pensando en tener hijos.
Se puede hacer un examen de sangre para ver si la persona porta el gen para esta enfermedad.
Se pueden hacer exámenes prenatales, como amniocentesis o muestras de vellosidades coriónicas, para buscar esta enfermedad en un bebé en desarrollo.
Vanier M. Disorders of sphingolipid metabolism. In: Fernandes J, Saudubray J-m, van den Berghe G, Walter JH, eds. Metabolic Diseases: Diagnosis and Treatment. 4th ed. New York, NY:Springer; 2006:chap 38.
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