LRP5 variant
osteoporosis-pseudoglioma
young osteoporosis
Journal
JCEM case reports
ISSN: 2755-1520
Titre abrégé: JCEM Case Rep
Pays: England
ID NLM: 9918609886906676
Informations de publication
Date de publication:
Oct 2024
Oct 2024
Historique:
received:
20
05
2024
medline:
23
9
2024
pubmed:
23
9
2024
entrez:
23
9
2024
Statut:
epublish
Résumé
Osteoporosis in children and young adults is relatively rare. Hereditary causes are often overlooked in the absence of a positive family history. We report a 29-year-old male presenting with recurrent fragility fractures since 6 years of age. Secondary causes, such as celiac disease, inflammatory disorders, and hypogonadism, were ruled out. Family history was negative for any bone disease. Exome sequencing revealed 2 variants of
Identifiants
pubmed: 39309619
doi: 10.1210/jcemcr/luae163
pii: luae163
pmc: PMC11414401
doi:
Types de publication
Case Reports
Journal Article
Langues
eng
Pagination
luae163Informations de copyright
© The Author(s) 2024. Published by Oxford University Press on behalf of the Endocrine Society.