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Congenital biotinidase deficiency – MRI findings in two cases
Congenital biotinidase deficiency is a rare inborn error of metabolism that most commonly presents in infantile age group. Diffusion changes on magnetic resonance imaging (MRI) are sparsely described in the literature. We are presenting diffusion-weighted MRI findings in two confirmed cases of conge...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Indian J Radiol Imaging |
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| Κύριοι συγγραφείς: | , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Wolters Kluwer - Medknow
2019
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6467045/ https://ncbi.nlm.nih.gov/pubmed/31000952 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ijri.IJRI_159_18 |
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