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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.
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http://dx.doi.org/10.1093/braincomms/fcad281 | DOI Listing |
BMC Neurol
August 2025
Department of Neurology, Peking University First Hospital, Beijing, China.
Background And Purpose: Heterozygous HTRA1-related cerebral small vessel disease (hHTRA1-CSVD) presents diagnostic challenges due to its clinical and imaging similarities with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) and sporadic cerebral small vessel disease (CSVD). Recently, the "chocolate chip sign" around the midbrain has been proposed as a potential imaging marker for hHTRA1-CSVD. However, the diagnostic value of similar findings around the pons remains unclear.
View Article and Find Full Text PDFBMJ Case Rep
August 2025
Pediatric Neurology, Indira Gandhi Institute of Child Health, Bengaluru, Karnataka, India.
Acute necrotising encephalopathy type 1 (ANE1) is a rare, autosomal dominant disorder caused by mutations in the gene, characterised by recurrent episodes of encephalopathy triggered by febrile illness. The hallmark neuroimaging feature typically involves bilateral symmetric thalamic lesions. Atypical findings, either clinical or neuroimaging-wise, can pose significant diagnostic challenges.
View Article and Find Full Text PDFJ Clin Res Pediatr Endocrinol
August 2025
İzmir Katip Çelebi University Faculty of Medicine, Pediatric Endocrinology Division, İzmir, Türkiye.
Carney Complex (CNC) is a rare autosomal dominant syndrome characterized by skin pigmentation abnormalities, endocrine tumors, and cardiac myxomas. This report presents an 11-year-old girl with a history of pontine glioma treated with chemotherapy and radiotherapy at 2.5 years of age, who presented with complaints of weight gain and short stature, along with syndromic features (multiple nevi around the mouth and nose, four café-au-lait spots, and bilateral clinodactyly of the fourth toes) identified during physical examination.
View Article and Find Full Text PDFLancet Reg Health Eur
August 2025
German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.
Background: Spinocerebellar ataxia type 3 (SCA3) is an autosomal dominantly inherited adult-onset disease. We aimed to describe longitudinal changes in clinical and biological findings and to identify predictors for clinical progression.
Methods: We used data from participants enrolled in the ESMI cohort collected between Nov 09, 2016 and July 18, 2023.
Curr Neurol Neurosci Rep
July 2025
Department of Neurology, Vivekananda Institute of Medical Sciences, Kolkata, West Bengal, India.
Purpose Of Review: Definitive diagnosis of multiple sclerosis (MS) requires exclusion of other central nervous system (CNS) disorders sharing similar clinical, pathological and radiological features. In this review we discuss some relatively uncommon disorders with special emphasis on their differentiation from MS clinically and radiologically. While most conditions have a demyelinating pathology, a few very important mimics may have a non-demyelinating pathology to merit some discussion.
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