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DOI: 10.4103/ijri.IJRI_159_18
Congenital biotinidase deficiency – MRI findings in two cases
Verantwortlicher Herausgeber dieser Rubrik:
Financial support and sponsorship Nil.
Abstract
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 congenital biotinidase deficiency in infantile age group with review of literature.
Publikationsverlauf
Artikel online veröffentlicht:
23. Juli 2021
© 2019. Indian Radiological Association. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).
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