Evidence map›Paper›PMID 41695731›Full record

ArticleWorld journal of orthopedics2026

Osteopathia striata with cranial sclerosis, associated with juvenile idiopathic arthritis: A case report and review of literature.

Alexandr A Yakovlev, Ekaterina V Gaidar, Evgeny N Suspitsin, Polina R Korzun, Mikhail M Kostik

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in World journal of orthopedics, 2026. 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

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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

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Alexandr A YakovlevDepartment of Pediatry, Saint-Petersburg State Pediatric Medical University, Saint Petersburg 194100, Sankt-Peterburg, Russia.
Ekaterina V GaidarDepartment of Pediatry, Saint-Petersburg State Pediatric Medical University, Saint Petersburg 194100, Sankt-Peterburg, Russia.
Evgeny N SuspitsinDepartment of Medical Genetics, Saint-Petersburg State Pediatric Medical University, Saint Petersburg 194100, Sankt-Peterburg, Russia.
Polina R KorzunDepartment of Medical Genetics, Saint-Petersburg State Pediatric Medical University, Saint Petersburg 194100, Sankt-Peterburg, Russia.
Mikhail M KostikDepartment of Pediatry, Saint-Petersburg State Pediatric Medical University, Saint Petersburg 194100, Sankt-Peterburg, Russia. kost-mikhail@yandex.ru.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOsteopathia striata with cranial stenosis (OSCS) is a rare genetic disorder (Mendelian Inheritance in Man: 300373) inherited in an X-linked dominant pattern. It is classified as a form of skeletal dysplasia and is characterized by linear striations of bone sclerosis, primarily affecting the long bones. OSCS may present as an isolated condition or as part of broader genetic conditions such as Horan-Beighton and Goltz syndromes. Thus far, approximately 100 cases have been reported. CASE SUMMARY: Herein, we report the case of an 11-year-old girl with OSCS in association with juvenile idiopathic arthritis (JIA). Osteopathia striata was suspected during the examination in a local healthcare facility due to arthritis. The patient was then transferred to the pediatric rheumatology clinic due to the inefficacy of the first-line systemic immunosuppressive therapy. Genetic analysis revealed a previously unreported

conclusionDiagnosis of OSCS can be challenging due to its rarity and phenotypic heterogeneity. The relationship between JIA and OSCS remains unclear. This case may raise awareness of OSCS.

Indexed as

AMER1 mutationCase reportGenetic disordersImaging studiesJuvenile idiopathic arthritisOsteopathia striata with cranial sclerosisSkeletal dysplasiaVoorhoeve disease

Identifiers

PMID41695731
PMCPMC12898134

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