Allgrove syndrome and motor neuron disease

Allgrove or triple A syndrome (AS or AAA) is a rare autosomal recessive syndrome with variable phenotype due to mutations in AAAS gene which encodes a protein called ALADIN. Generally, it’s characterized by of adrenal insufficiency in consequence of adrenocorticotropic hormone (ACTH) resistance, bes...

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Dettagli Bibliografici
Pubblicato in:Neurol Int
Autori principali: de Freitas, Marcos R.G., Orsini, Marco, Araújo, Alexandra Prufer de Queiroz Campos, Jr., Luiz João Abraão, Barbosa, Gilberto Miranda, França, Marcondes C., Correia, Luan, Bastos, Victor Hugo, Trajano, Eduardo, Jr., Mauricio da Sant’Anna
Natura: Artigo
Lingua:Inglês
Pubblicazione: PAGEPress Publications, Pavia, Italy 2018
Soggetti:
Case Report
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6050446/
https://ncbi.nlm.nih.gov/pubmed/30069287
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4081/ni.2018.7436
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