AI Article Synopsis

  • Pontine autosomal dominant microangiopathy and leukoencephalopathy is a hereditary condition linked to small vessel diseases affecting the brain, marked by small infarctions in the pons region.
  • Researchers conducted genetic sequencing and clinical assessments on a family with this undiagnosed condition and identified a specific genetic variant that confirmed the diagnosis in two other patients.
  • A notable radiological feature termed the "raisin bread sign" was discovered, characterized by multiple oval small infarctions in the pons, which corresponds with specific pathological changes observed postmortem.

Article Abstract

Pontine autosomal dominant microangiopathy and leukoencephalopathy is one of hereditary cerebral small vessel diseases caused by pathogenic variants in 3'UTR and characterized by multiple small infarctions in the pons. We attempted to establish radiological features of this disease. We performed whole exome sequencing and Sanger sequencing in one family with undetermined familial small vessel disease, followed by clinicoradiological assessment and a postmortem examination. We subsequently investigated clinicoradiological features of patients in a juvenile cerebral vessel disease cohort and searched for radiological features similar to those found in the aforementioned family. Sanger sequencing was performed in selected cohort patients in order to detect variants in the same gene. An identical variant in the 3'UTR was observed in two patients with familial small vessel disease and the two selected patients, thereby confirming the pontine autosomal dominant microangiopathy and leukoencephalopathy diagnosis. Furthermore, postmortem examination showed that the distribution of thickened media tunica and hyalinized vessels was different from that in lacunar infarctions. The appearance of characteristic multiple oval small infarctions in the pons, which resemble raisin bread, enable us to make a diagnosis of pontine autosomal dominant microangiopathy and leukoencephalopathy. This feature, for which we coined the name 'raisin bread sign', was also correlated to the pathological changes.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10636559PMC
http://dx.doi.org/10.1093/braincomms/fcad281DOI Listing

Publication Analysis

Top Keywords

pontine autosomal
16
autosomal dominant
16
dominant microangiopathy
16
microangiopathy leukoencephalopathy
16
small vessel
12
vessel disease
12
'raisin bread
8
bread sign'
8
small infarctions
8
infarctions pons
8

Similar Publications

A congenital neurologic disorder affected a herd of Tabapuã cattle. Of 98 newborn calves, 12 (12%) were affected; they were sired by 3 related bulls. This frequency suggested a genetic disorder caused by an autosomal recessive gene.

View Article and Find Full Text PDF

Leukoencephalopathy with vanishing white matter is a new autosomal recessive inherited disorder disease entity. It is a chronic disease with a progressive course and episodes of exacerbation, the prevalence of which is still unknown. This disease usually occurs in children and is rare, particularly in the non-Caucasian population.

View Article and Find Full Text PDF

Progressive Apraxia of Speech as a Manifestation of Spinocerebellar Ataxia 2: Case Report.

Neurol Genet

December 2024

From the Neurology (A.M.B., L.M.J., R.G., J.M.M.-T., K.A.J., H.B.); Speech Pathology (G.M., J.S., J.R.D., H.C., R.L.U.); Psychology (M.M.M.); and Radiology (J.L.W.), Mayo Clinic, Rochester, MN.

Objectives: To describe a case of spinocerebellar ataxia presenting with progressive apraxia of speech (AOS).

Methods: A 54-year-old man with progressive speech changes was seen clinically and referred to our observational research program on degenerative speech and language disorders. He underwent detailed speech-language and neurologic assessments and multimodal neuroimaging studies.

View Article and Find Full Text PDF

EAST syndrome - Epilepsy, Ataxia, Sensorineural hearing loss, and renal Tubulopathy - is an autosomal recessive disorder affecting the potassium channel in the brain, inner ear, and basolateral membrane of the distal nephron of the kidney. The mutation in the gene is responsible for defective potassium transport in those locations, resulting in seizures, hearing loss, and hypokalemia. Imaging findings of this disease are typical, such as cerebellar hypoplasia and signal changes in bilateral dentate nuclei, midbrain, pons, and medulla, with variable restricted diffusion due to intramyelinic edema.

View Article and Find Full Text PDF

Monogenic causes of cerebral small vessel disease and stroke.

Handb Clin Neurol

September 2024

Translational Centre for Neurovascular Disorders, Hôpital Lariboisière AP-HP, Paris, France; Paris-Cité University, Inserm U1141 NeuroDiderot, Paris, France.

Article Synopsis
  • * Key indicators for genetic screening include early onset of the disease, family history, and a significant presence of cSVD imaging markers despite a low vascular risk profile.
  • * Currently, there are several known genes associated with Mendelian cSVDs, but less than 15% of patients with suspected genetic issues have identified pathogenic variants, indicating that more genetic factors are likely yet to be discovered.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!