18q deletion in a cystic fibrosis infant, increased morbidity and challenge for correct treatment choices: a case report

Cystic Fibrosis (CF) is the most frequent recessive disease of Caucasian patients. Association with other diseases or syndromes has previously been reported. Co-morbidity may be a challenge for clinicians, who have to face more severe problems. We have described a CF infant, F508del homozygote, diag...

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Detalles Bibliográficos
Autores principales: Spinelli, Elide, Timpano, Silviana, Fogazzi, Annalisa, Dester, Silvia, Milianti, Susanna, Padoan, Rita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120749/
https://www.ncbi.nlm.nih.gov/pubmed/21586141
http://dx.doi.org/10.1186/1824-7288-37-22

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120749/
https://www.ncbi.nlm.nih.gov/pubmed/21586141
http://dx.doi.org/10.1186/1824-7288-37-22

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