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Rud's syndrome
Rud's syndrome is a rare autosomal recessive hereditary disorder characterized by congenital ichthyosis, epilepsy, dwarfism, sexual infantilism, polyneuritis, and macrocytic anemia. We report here an interesting case of this disorder in an 18-year-old girl for its rarity and academic interest.
Autores principales: | Pavani, K., Reddy, B. S. N., Singh, B. Amar |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4030348/ https://www.ncbi.nlm.nih.gov/pubmed/24860755 http://dx.doi.org/10.4103/2229-5178.131093 |
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