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Unusual Presentation of Galactosemia in a Child: Musculoskeletal Manifestations
Galactosemia is an autosomal recessive inherited disease of galactose metabolism. In this report, a galactosemia case with unusual presentation has been presented. We reported a child boy with galactosemia presented with arthralgia, hands deformity and decreased bone mineral density.
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
The Mediterranean Journal of Rheumatology (MJR)
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7045964/ https://www.ncbi.nlm.nih.gov/pubmed/32185352 http://dx.doi.org/10.31138/mjr.30.2.123 |