Alpha(1)-Antitrypsin Deficiency: Transition of Care for the Child With AAT Deficiency into Adulthood

Importance: Alpha(1)-antitrypsin (AAT) deficiency is a common, but an underdiagnosed genetic condition, affecting 1 in 1500 individuals. It can present insidiously with liver disease in children. Although clinical practice guidelines exist for the management of AAT deficiency, especially with regard...

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Detalles Bibliográficos
Autores principales: Lin, Henry C., Kasi, Nagraj, Quiros, J. Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6696823/
https://www.ncbi.nlm.nih.gov/pubmed/30421678
http://dx.doi.org/10.2174/1573396314666181113094517

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6696823/
https://www.ncbi.nlm.nih.gov/pubmed/30421678
http://dx.doi.org/10.2174/1573396314666181113094517

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