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Erschienen in: Osteoporosis International 11/2017

02.09.2017 | Case Report

Clinical and biochemical response to neridronate treatment in a patient with osteoporosis-pseudoglioma syndrome (OPPG)

verfasst von: M. Celli, P. D’Eufemia, P. Persiani, A. Turchetti, A. Febbo, Y. D’Alfonso, L. Celli, A. Zambrano

Erschienen in: Osteoporosis International | Ausgabe 11/2017

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Abstract

Osteoporosis-pseudoglioma syndrome (OPPG) is a rare autosomal recessive syndrome characterized by juvenile-onset osteoporosis and ocular abnormalities due to a low-density lipoprotein receptor-related protein 5 (LRP5) gene mutation. Treatment with bisphosphonates, particularly with pamidronate and risedronate, has been reported to be of some efficacy in this condition. We report on a patient with OPPG due to an LRP5 gene mutation, who showed an encouraging response after a 36-month period of neridronate therapy. We report a case of a patient treated with bisphosphonates. Bisphosphonates should be administered in OPPG patients as a first-line therapy during early childhood.
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Metadaten
Titel
Clinical and biochemical response to neridronate treatment in a patient with osteoporosis-pseudoglioma syndrome (OPPG)
verfasst von
M. Celli
P. D’Eufemia
P. Persiani
A. Turchetti
A. Febbo
Y. D’Alfonso
L. Celli
A. Zambrano
Publikationsdatum
02.09.2017
Verlag
Springer London
Erschienen in
Osteoporosis International / Ausgabe 11/2017
Print ISSN: 0937-941X
Elektronische ISSN: 1433-2965
DOI
https://doi.org/10.1007/s00198-017-4214-x

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