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

A family with a variant form of primary hypertrophic osteoarthropathy restricted to the lower extremities.

Joint bone spine - 1 Jun 2003

Seggewiss Ruth, Hess Thomas, Fiehn Christoph

Abstract excerpt

We report a case of a family with a variant form of primary hypertrophic osteoarthropathy (HOA) restricted to the lower extremities without digital clubbing or cutaneous changes. Three family members suffered from pain, swelling and hyperhidrosis of both feet. X-rays showed destruction and osteop...

Read the complete abstract on PubMed

Topics

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

Share to Genetic Predisposition to Disease
Share to Pedigree
Share to Radiography

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 12814767
DOI: 10.1016/s1297-319x(03)00048-4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-12814767-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 11 closest

A family with a variant form of primary hypertrophic osteoarthropathy restricted to the lower extremities.PMID 12814767Read ↗

Touraine-Solente-Gole syndrome: pathogenic variant in SLCO2A1 presented with polyarthralgia and digital clubbingSemantic proximity Read ↗

Primary hypertrophic osteoarthropathy: a new family supporting genetic heterogeneity.Semantic proximity Read ↗

Primary Hypertrophic Osteoarthropathy: An Update on Patient Features and TreatmentSemantic proximity Read ↗

Primary hypertrophic osteoarthropathy caused by homozygous deletion in HPGD gene in a family: changing clinical and radiological findings with long-term follow-up.Semantic proximity Read ↗

A novel mutation in the HPGD gene causing primary hypertrophic osteoarthropathy with digital clubbing in a Pakistani family.Semantic proximity Read ↗

Camurati-Engelmann disease (progressive diaphyseal dysplasia) in a Moroccan family.Semantic proximity Read ↗

Primary hypertrophic osteoarthropathy with severe arthralgia identified by gene mutation of SLCO2A1.Semantic proximity Read ↗

Primary hypertrophic osteoarthropathy with digital clubbing and palmoplantar hyperhidrosis caused by 15-PGHD/HPGD loss-of-function mutations.Semantic proximity Read ↗

A case of primary hypertrophic osteoarthropathy: Management considerations.Semantic proximity Read ↗

Hereditary isolated metatarsophalangeal arthritis.Semantic proximity Read ↗

Mutations in the prostaglandin transporter encoding gene SLCO2A1 cause primary hypertrophic osteoarthropathy and isolated digital clubbing.Semantic proximity Read ↗

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