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

“Ears of the Lynx” MRI Sign Is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia

1 Jan 2019

Abstract excerpt

BACKGROUND AND PURPOSE: gene, causing Spastic Paraplegia type 11 (SPG11). This sign corresponds to long T1 and T2 values in the forceps minor of the corpus callosum, which appears hyperintense on FLAIR and hypointense on T1-weighted images. Our purpose was to determine the sensitivity and specificity of the ears of the lynx MR imaging sign for genetic cases compared with common potential mimics. MATERIALS AND...

Read the complete abstract on PubMed

Topics

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

Share to Amyotrophic Lateral Sclerosis Research
Share to Hereditary Neurological Disorders
Share to Peripheral Neuropathies and Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 30606727
DOI: 10.3174/ajnr.a5935

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

“Ears of the Lynx” MRI Sign Is Associated with SPG11 and SPG15 Hereditary Spastic ParaplegiaPMID 30606727Read ↗

Forceps minor region signal abnormality "ears of the lynx": an early MRI finding in spastic paraparesis with thin corpus callosum and mutations in the spatacsin gene (SPG11) on chromosome 15.Semantic proximity Read ↗

Cross sign T2 hyperintensities in atrophic spinal cord of hereditary spastic paraplegia type 5Semantic proximity Read ↗

'Ears of the Lynx' sign: an important and useful MRI clue for diagnosis of hereditary spastic paraplegia (HSP) caused by mutation in SPG 15 gene.Semantic proximity Read ↗

SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum.Semantic proximity Read ↗

Subtle Imaging Findings Aid the Diagnosis of Adolescent Hereditary Spastic Paraplegia and Ataxia.Semantic proximity Read ↗

Neuroimaging patterns in paediatric onset hereditary spastic paraplegias.Semantic proximity Read ↗

White and grey matter abnormalities in patients withSPG11mutationsSemantic proximity Read ↗

Expanding the muscle imaging spectrum in dysferlinopathy: description of an outlier population from the classical MRI pattern.Semantic proximity Read ↗

Neuroimaging in Hereditary Spastic Paraplegias: Current Use and Future PerspectivesSemantic proximity Read ↗

Late-Onset Tay-Sachs Disease With SMALED-Like Muscle MRI Pattern Despite a Distinct Clinical Phenotype.Semantic proximity Read ↗

Monozygotic twins with a new compound heterozygous SPG11 mutation and different disease expression.Semantic proximity Read ↗

Diffusion tensor imaging in SPG11- and SPG4-linked hereditary spastic paraplegia.Semantic proximity Read ↗

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