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

Unusual neuroradiological features in Schinzel-Giedion syndrome: a novel case.

Clinical dysmorphology - 1 Jul 2012

Lestner Jodi Marianne, Chong Wui K, Offiiah Amaka, Kefas Jonathan, Vandersteen Anthony M

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Abnormalities, Multiple
Share to Carrier Proteins
Share to Craniofacial Abnormalities
Share to Hand Deformities, Congenital

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Intellectual Disability

Share to Malformations of Cortical Development

Share to Nails, Malformed

Share to Seizures

Source

Identifiers

PMID: 22473152
DOI: 10.1097/MCD.0b013e3283518f1e

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 20 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Unusual neuroradiological features in Schinzel-Giedion syndrome: a novel case.PMID 22473152Read ↗

Schinzel–Giedion syndrome: a novel case, review and revised diagnostic criteriaSemantic proximity Read ↗

Atypical presentation of Waardenburg's syndrome type II.Semantic proximity Read ↗

Schinzel-Giedion syndrome: autopsy report and additional clinical manifestations.Semantic proximity Read ↗

Atypical presentation of vanishing white matter disease.Semantic proximity Read ↗

Schwannomatosis: the overlooked neurofibromatosis?Semantic proximity Read ↗

Sturge-Weber-Klippel-Trenaunay syndrome: what's in a name?Semantic proximity Read ↗

SPENCD Presenting with Evans Phenotype and Clinical Response to JAK1/2 Inhibitors-a Report of 2 Cases.Semantic proximity Read ↗

Imaging findings in a child with Loeys-Dietz syndrome.Semantic proximity Read ↗

Neurofibromatosis type 1 with undescribed osseous abnormalities: new features?Semantic proximity Read ↗

Muir-Torre Syndrome and Central Nervous System Malignancy: Highlighting an Uncommon Association.Semantic proximity Read ↗

Preoperative MRI diagnosis of lhermitte-duclos disease: Case report with associated enlarged vessel and syrinxSemantic proximity Read ↗

Brain tumors in Li-Fraumeni syndrome: a commentary and a case of a gliosarcoma patient.Semantic proximity Read ↗

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