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

A case of extensive hyperostosis frontalis interna in an 87-year-old female human cadaver.

Clinical anatomy (New York, N.Y.) - 1 Apr 2008

Talarico Ernest F, Prather Andrew D, Hardt Kevin D

Abstract excerpt

Hyperostosis frontalis interna (HFI) is a condition that involves thickening of the inner surface of the frontal bone with sparing of the midline. Little is known about the etiology and clinical presentation of HFI. We report unusual findings in a woman with extensive Type D hyperostosis of the frontal bone and a large hyperostotic nodule in the parietal bone with impingement on the precentral gyrus,...

Read the complete abstract on PubMed

Topics

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

Share to Aged, 80 and over
Share to Phenotype
Share to Skull

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 18351650
DOI: 10.1002/ca.20613

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A case of extensive hyperostosis frontalis interna in an 87-year-old female human cadaver.PMID 18351650Read ↗

Hyperostosis frontalis interna as a novel finding in Unverricht-Lundborg disease.Semantic proximity Read ↗

Benign fibro-osseous lesions of the craniofacial complex. A review.Semantic proximity Read ↗

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

Temporal Lobe Malformations in Achondroplasia: Expanding the Brain Imaging Phenotype Associated with FGFR3-Related Skeletal Dysplasias.Semantic proximity Read ↗

Fibrous Dysplasia Presenting as a Gingival Mass: A Rare Clinical PresentationSemantic proximity Read ↗

Frontal bone fibrous dysplasia in a 6-months-old boy: A distinctive entity.Semantic proximity Read ↗

Pathogenesis and treatment of a giant occipital bone defect with meningoencephalocele in an NF1 child: case report and review of the literature.Semantic proximity Read ↗

Craniovascular traits and braincase morphology in craniosynostotic human skulls.Semantic proximity Read ↗

Facial nerve decompression via middle fossa approach for hyperostosis cranialis interna: a feasible therapeutic approach.Semantic proximity Read ↗

Temporal and occipital lobe features in children with hypochondroplasia/FGFR3 gene mutation.Semantic proximity Read ↗

A unique case of progressive hemifacial microsomia or Parry-Romberg syndrome associated with limb and brain anomalies with normal neurological findings: A review of the literature.Semantic proximity Read ↗

Calvarial mass as a presenting feature of neurofibromatosis type 2 in a pediatric patient.Semantic proximity Read ↗

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