Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Diagnosis of Klippel-Trenaunay syndrome and extensive heterotopic ossification in a patient with a femoral fracture: a case report and literature review.

BMC musculoskeletal disorders - 11 Apr 2020

Zhu Wanbo, Xie Kai, Yang Jiazhao, Li Li, Wang Xujin, Xu Lei, Fang Shiyuan

Abstract excerpt

BACKGROUND: Klippel-Trenaunay syndrome (KTS) is a rare complex vessel malformation syndrome characterized by venous varicosities, capillary malformations, and limb hypertrophy. However, extensive heterotopic ossification (HO) secondary to this syndrome is extremely rare. CASE PRESENTATION: We report the case of a patient with previously undiagnosed KTS and extensive HO who presented with a femoral fracture...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Forkhead Box Protein O1
Share to Imaging, Three-Dimensional

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Ossification, Heterotopic

Share to Tomography, X-Ray Computed

Source

Open in PubMed Open full text

Identifiers

PMID: 32278353
DOI: 10.1186/s12891-020-03224-2
PMCID: PMC7149888

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Diagnosis of Klippel-Trenaunay syndrome and extensive heterotopic ossification in a patient with a femoral fracture: a case report and literature review.PMID 32278353Read ↗

Klippel-Trenaunay Syndrome.Semantic proximity Read ↗

Idiopathic avascular necrosis of the femoral heads in five members of a Moroccan family.Semantic proximity Read ↗

The Klippel-Trénaunay Syndrome in 2022: Unravelling Its Genetic and Molecular Profile and Its Link to the Limb Overgrowth Syndromes.Semantic proximity Read ↗

Current Understanding of Epidemiology, Pathophysiology, and Management of Atypical Femur Fractures.Semantic proximity Read ↗

Venous malformation may be a feature of EXT1-related hereditary multiple exostoses: A report of two unrelated probands.Semantic proximity Read ↗

Multiple osteochondromas.Semantic proximity Read ↗

Legg-Calve-Perthes disease: etiology, pathogenesis, and biology.Semantic proximity Read ↗

Klippel-Trenaunay syndromeSemantic proximity Read ↗

Etiology and Pathogenesis of OsteochondrosisSemantic proximity Read ↗

Cavernous hemangioma of the knee, causing pain following a fall in a 5-year-old girl: A case report.Semantic proximity Read ↗

Combined capillary-venous-lymphatic malformations without overgrowth in patients with Klippel-Trénaunay syndrome.Semantic proximity Read ↗

Germline VWF/MPRIP and somatoplasm FGA variants synergically confer susceptibility to non-traumatic osteonecrosis of the femoral headSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.