Pycnodysostosis: natural history and ...
Document type :
Article dans une revue scientifique: Article original
DOI :
PMID :
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Title :
Pycnodysostosis: natural history and management guidelines from 27 french cases and a literature review
Author(s) :
Bizaoui, Varoona [Auteur]
Michot, Caroline [Auteur]
Baujat, Genevieve [Auteur]
Amouroux, Cyril [Auteur]
Baron, Sabine [Auteur]
Capri, Yline [Auteur]
Cohen-Solal, Martine [Auteur]
Collet, Corinne [Auteur]
Dieux, Anne [Auteur]
Genevieve, David [Auteur]
Isidor, Bertrand [Auteur]
Monnot, Sophie [Auteur]
Rossi, Massimiliano [Auteur]
Rothenbuhler, Anya [Auteur]
Schaefer, Elise [Auteur]
Cormier-Daire, Valerie [Auteur]
Michot, Caroline [Auteur]
Baujat, Genevieve [Auteur]
Amouroux, Cyril [Auteur]
Baron, Sabine [Auteur]
Capri, Yline [Auteur]
Cohen-Solal, Martine [Auteur]
Collet, Corinne [Auteur]
Dieux, Anne [Auteur]
![refId](/themes/Mirage2//images/idref.png)
Genevieve, David [Auteur]
Isidor, Bertrand [Auteur]
Monnot, Sophie [Auteur]
Rossi, Massimiliano [Auteur]
Rothenbuhler, Anya [Auteur]
Schaefer, Elise [Auteur]
Cormier-Daire, Valerie [Auteur]
Journal title :
Clinical Genetics
Abbreviated title :
Clin. Genet.
Publication date :
2019-06-25
ISSN :
1399-0004
Keyword(s) :
bone fragility
CTSK
osteosclerosis
pycnodysostosis
CTSK
osteosclerosis
pycnodysostosis
HAL domain(s) :
Sciences du Vivant [q-bio]
English abstract : [en]
Pycnodysostosis is a lysosomal autosomal recessive skeletal dysplasia characterized by osteosclerosis, short stature, acro-osteolysis, facial features and an increased risk of fractures. The clinical heterogeneity of the ...
Show more >Pycnodysostosis is a lysosomal autosomal recessive skeletal dysplasia characterized by osteosclerosis, short stature, acro-osteolysis, facial features and an increased risk of fractures. The clinical heterogeneity of the disease and its rarity make it difficult to provide patients an accurate prognosis, as well as appropriate care and follow-up. French physicians from the OSCAR network have been asked to fill out questionnaires collecting molecular and clinical data for 27 patients issued from 17 unrelated families. All patients showed short stature (mean = -3.5 SD) which was more severe in females (P = .006). The mean fracture rate was moderate (0.21 per year), with four fractures in total average. About 75% underwent at least one surgery, with an average number of 2.1 interventions per patient. About 50% required non-invasive assisted ventilation due to sleep apnea (67%). About 29% showed psychomotor difficulties and 33% needed a school assistant or adapted schooling. No patient had any psychological evaluation or follow-up. Molecular data were available for 14 families. Growth hormone administration was efficient on linear growth in 40% of cases. We propose several axis of management, such as systematic cerebral MRI for Chiari malformation screening at diagnosis and regular psychological follow-up.Show less >
Show more >Pycnodysostosis is a lysosomal autosomal recessive skeletal dysplasia characterized by osteosclerosis, short stature, acro-osteolysis, facial features and an increased risk of fractures. The clinical heterogeneity of the disease and its rarity make it difficult to provide patients an accurate prognosis, as well as appropriate care and follow-up. French physicians from the OSCAR network have been asked to fill out questionnaires collecting molecular and clinical data for 27 patients issued from 17 unrelated families. All patients showed short stature (mean = -3.5 SD) which was more severe in females (P = .006). The mean fracture rate was moderate (0.21 per year), with four fractures in total average. About 75% underwent at least one surgery, with an average number of 2.1 interventions per patient. About 50% required non-invasive assisted ventilation due to sleep apnea (67%). About 29% showed psychomotor difficulties and 33% needed a school assistant or adapted schooling. No patient had any psychological evaluation or follow-up. Molecular data were available for 14 families. Growth hormone administration was efficient on linear growth in 40% of cases. We propose several axis of management, such as systematic cerebral MRI for Chiari malformation screening at diagnosis and regular psychological follow-up.Show less >
Language :
Anglais
Audience :
Internationale
Popular science :
Non
Administrative institution(s) :
Université de Lille
Collections :
Submission date :
2021-09-02T07:02:07Z