A complicated association between two different genetic rare disorders: cystic fibrosis and spinal muscular atrophy
Minerva Pediatr (Torino)
.
2022 Dec;74(6):797-799.
doi: 10.23736/S2724-5276.19.05614-7.
Epub 2021 Apr 2.
Authors
Marta Palma
1
,
Simona Spadarella
2
,
Bernadette Donnarumma
2
,
Giada Zollo
2
,
Francesco Nunziata
2
,
Chiara Cimbalo
2
,
Alice Castaldo
2
,
Paolo Buonpensiero
2
,
Gaetano Terrone
3
,
Antonio Varone
4
,
Antonella Tosco
5
,
Angela Sepe
5
,
Valeria Raia
5
Affiliations
1
Section of Pediatrics, Department of Medical and Translational Sciences, University of Naples Federico II, Naples, Italy - marta.palma@unina.it.
2
Section of Pediatrics, Department of Medical and Translational Sciences, University of Naples Federico II, Naples, Italy.
3
Unit of Child Neuropsychiatry, Department of Medical and Translational Sciences, University of Naples Federico II, Naples, Italy.
4
Department of Neurosciences, Santobono-Pausilipon Children's Hospital, Naples, Italy.
5
Regional Cystic Fibrosis Center, Pediatric Unit, Department of Medical and Translational Sciences, University of Naples Federico II, Naples, Italy.
PMID:
33820398
DOI:
10.23736/S2724-5276.19.05614-7
No abstract available
MeSH terms
Cystic Fibrosis* / complications
Cystic Fibrosis* / genetics
Humans
Mass Screening
Muscular Atrophy, Spinal* / genetics
Rare Diseases / genetics