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Oral manifestation and dental treatment of pediatric patient with beta-mannosidosis: A case report
β-mannosidosis is a rare autosomal recessive lysosomal storage disease of glycoprotein catabolism caused by a deficiency of β-mannosidase. Clinical presentation includes intellectual deficits, hearing loss, and recurrent respiratory infections. This report describes the dental treatment and follow-u...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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SAGE Publications
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8679027/ https://www.ncbi.nlm.nih.gov/pubmed/34925842 http://dx.doi.org/10.1177/2050313X211065796 |