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Clinical and genetic characterization of a Chanarin Dorfman Syndrome patient born to diseased parents
BACKGROUND: Chanarin Dorfman Syndrome (CDS) is a rare autosomal recessive disorder characterized by ichthyosiform non-bullous erythroderma and variable involvement of the liver and the neuromuscular system. In CDS patients, the accumulation of neutral lipids inside cytoplasmic lipid droplets has bee...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2018
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5975656/ https://www.ncbi.nlm.nih.gov/pubmed/29843625 http://dx.doi.org/10.1186/s12881-018-0610-0 |