Low Psychosine in Krabbe Disease with Onset in Late Infancy: A Case Report

Krabbe disease (KD) is a rare inherited neurodegenerative disorder caused by a deficiency in galactocerebrosidase enzyme activity, which can present in early infancy, requiring an urgent referral for hematopoietic stem cell transplantation, or later in life. Newborn screening (NBS) for KD requires i...

Descripción completa

Detalles Bibliográficos
Autores principales: Corre, Camille S., Matern, Dietrich, Pellegrino, Joan E., Saavedra-Matiz, Carlos A., Orsini, Joseph J., Thompson-Stone, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162352/
https://www.ncbi.nlm.nih.gov/pubmed/34071213
http://dx.doi.org/10.3390/ijns7020028

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162352/
https://www.ncbi.nlm.nih.gov/pubmed/34071213
http://dx.doi.org/10.3390/ijns7020028

Ejemplares similares