Evidence map›Paper›PMID 40486414›Full record

ArticleCureus2025

Idiopathic Juvenile Osteoporosis Diagnosed in Adulthood: The First Documented Case in Georgia.

Giorgi Akhvlediani, Nana Nakaidze, Elene Dzodzuashvili, Nino Gabidzashvili, Elene Dopidze, Ana Mikaberidze, Kristine Ambriashvili

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors.

Giorgi AkhvledianiPulmonary and Critical Care Medicine, Tbilisi State Medical University, Tbilisi, GEO.
Nana NakaidzeEndocrinology, Diabetes and Metabolism, American Hospital Tbilisi, Tbilisi, GEO.
Elene DzodzuashviliInternal Medicine, Vian Hospitals, Tbilisi, GEO.
Nino GabidzashviliEndocrinology, Diabetes and Metabolism, American Hospital Tbilisi, Tbilisi, GEO.
Elene DopidzeEndocrinology, Diabetes and Metabolism, American Hospital Tbilisi, Tbilisi, GEO.
Ana MikaberidzeEndocrinology, Diabetes and Metabolism, American Hospital Tbilisi, Tbilisi, GEO.
Kristine AmbriashviliEndocrinology, Diabetes and Metabolism, American Hospital Tbilisi, Tbilisi, GEO.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Idiopathic juvenile osteoporosis (IJO) is a rare metabolic bone disorder characterized by bone fragility in otherwise healthy children and adolescents, with typical onset before puberty. To our knowledge, this represents the first documented case of IJO in Georgia, with a delayed diagnosis in adulthood despite a clinical history suggestive of earlier onset. A 24-year-old male with a history of childhood nephrolithiasis and intermittent vitamin D deficiency presented with progressive bone pain, joint crepitus, and worsening mobility. Imaging revealed severe osteopenia and osteoporosis, prompting an extensive metabolic and endocrine evaluation. Laboratory findings were largely unremarkable aside from episodic hypercalciuria, normal parathyroid hormone levels, and fluctuating vitamin D levels. Major secondary causes, including malignancy, hyperparathyroidism, thyroid dysfunction, chronic inflammatory disease, and malabsorption syndromes, were ruled out. A diagnosis of IJO was made by exclusion. The patient was started on calcium and vitamin D supplementation with close monitoring. This case highlights the diagnostic challenges of IJO when presentation extends into adulthood and underscores the importance of considering this condition in young adults with unexplained bone fragility, particularly in regions where it remains undocumented.

Indexed as

a case reportbone densityidiopathic juvenile osteoporosismarkers of bone metabolismmetabolic endocrinologyparathyroid hormone (pth)

Identifiers

PMID40486414
PMCPMC12144662

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