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Lysosomal Acid Lipase Deficiency: Report of Five Cases across the Age Spectrum

Lysosomal acid lipase (LAL) deficiency is an autosomal recessive lysosomal storage disorder caused by mutations in the LIPA gene that leads to premature organ damage and mortality. We present retrospective data from medical records of 5 Brazilian patients, showing the broad clinical spectrum of the...

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Dettagli Bibliografici
Pubblicato in:Case Rep Pediatr
Autori principali: Curiati, Marco Antonio, Kyosen, Sandra Obikawa, Pereira, Vanessa Gonçalves, Patrício, Francy Reis da Silva, Martins, Ana Maria
Natura: Artigo
Lingua:Inglês
Pubblicazione: Hindawi 2018
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5828415/
https://ncbi.nlm.nih.gov/pubmed/29527374
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2018/4375434
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