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Metabolic Treatment of Wolfram Syndrome

Wolfram Syndrome (WS) is a very rare genetic disorder characterized by several symptoms that occur from childhood to adulthood. Usually, the first clinical sign is non-autoimmune diabetes even if other clinical features (optic subatrophy, neurosensorial deafness, diabetes insipidus) may be present i...

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Detalles Bibliográficos
Autores principales: Iafusco, Dario, Zanfardino, Angela, Piscopo, Alessia, Curto, Stefano, Troncone, Alda, Chianese, Antonietta, Rollato, Assunta Serena, Testa, Veronica, Iafusco, Fernanda, Maione, Giovanna, Pennarella, Alessandro, Boccabella, Lucia, Ozen, Gulsum, Palma, Pier Luigi, Mazzaccara, Cristina, Tinto, Nadia, Miraglia del Giudice, Emanuele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8910219/
https://www.ncbi.nlm.nih.gov/pubmed/35270448
http://dx.doi.org/10.3390/ijerph19052755

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