@misc{10481/75988,
year = {2022},
month = {6},
url = {http://hdl.handle.net/10481/75988},
abstract = {Hajdu–Cheney syndrome is a rare genetic disease. Its main features include phenotypic
variability, age-dependent progression and the presence of acroosteolysis of the distal phalanges and
generalized osteoporosis, which have significant disabling potential. Currently, there is no effective
curative treatment, so nursing care is essential to ensure the maintenance of the quality of life of these
patients. The main objective of this study was to establish a specific standardized nursing care plan
using the NANDA–NIC–NOC taxonomy. The application of a care plan as such would improve
the quality of life of patients affected by this rare disease, will contribute to increasing healthcare
professionals’ knowledge on this matter and will support future studies on this disease.},
publisher = {MDPI},
keywords = {Rare disease},
keywords = {Hajdu-Cheney syndrome},
keywords = {Nursing care plan},
keywords = {Acroosteolysis},
keywords = {NOTCH2},
keywords = {Clinical practice},
keywords = {Healthcare},
title = {Nursing Care Plan for Patients with Hajdu–Cheney Syndrome},
doi = {10.3390/ijerph19127489},
author = {Cortés Martín, Jonathan and Díaz Rodríguez, Consuelo Lourdes and Piqueras Sola, Beatriz and Sánchez García, Juan Carlos and Rodríguez Blanque, Raquel},
}