Cargando…
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...
| Autores principales: | , , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2011
|
| Materias: | |
| 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 |