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
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

luae163

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the Endocrine Society.

Auteurs

Nupoor Vaghasia (N)

Institute of Endocrinology and Diabetes, Max Healthcare, Saket, New Delhi 110017, India.

Aditya Dutta (A)

Institute of Endocrinology and Diabetes, Max Healthcare, Saket, New Delhi 110017, India.

Ambrish Mithal (A)

Institute of Endocrinology and Diabetes, Max Healthcare, Saket, New Delhi 110017, India.

Classifications MeSH