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CT features of Wolman disease (lysosomal acid lipase enzyme deficiency) – A case report
Wolman disease is a lethal rare autosomal recessive disorder defined by the deficiency of acid lipase enzyme. The disease is a lysosomal storage disease. Multiple organs such as adrenal glands, liver, spleen, bone marrow, small bowel loops, and abdominal lymph nodes are infiltrated by the deposition...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Elsevier
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8349914/ https://www.ncbi.nlm.nih.gov/pubmed/34401013 http://dx.doi.org/10.1016/j.radcr.2021.06.084 |