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1.
Brain Dev ; 43(3): 448-453, 2021 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-33229101

RESUMO

BACKGROUND: Pallister-Killian syndrome (PKS) is a rare disorder caused by the mosaic tetrasomy of chromosome 12p, and is characterized by facial dysmorphism, developmental delay, hypotonia and seizures. RESULTS: We report a patient with PKS showing unique polymicrogyria with calcification. He had delayed development and dysmorphic facial features including frontal bossing, hypertelorism, and high arched palate at 6 months of age. Neuroimaging revealed unilateral polymicrogyria with spot calcifications, which predominantly affected the right perisylvian region. Chromosome G-banding showed the karyotype 46,XY, however, array-based comparative genomic hybridization analysis showed mosaic duplication of chromosome 12p, in which CCND2, which encodes cyclin D2 and is a downstream mediator of PI3K-AKT pathway, is located. Supernumerary chromosome of 12p was detected in 58% of buccal mucosa cells by the interphase fluorescence in situ hybridization analysis using chromosome 12 centromere-specific D12Z3 probe. The diagnosis of PKS was made based on distinctive clinical features of our patient and the results of cytogenetic analyses. CONCLUSION: This report is, to our knowledge, the first case of a patient with PKS who clearly demonstrates polymicrogyria colocalized with calcifications, as shown by CT scans and MRI, and suggests that a patient with PKS could show structural brain anomalies with calcification. We assume that somatic mosaicism of tetrasomy could cause asymmetrical polymicrogyria in our patient, and speculate that increased dosages of CCND2 at chromosome 12p might be involved in the abnormal neuronal migration in PKS.


Assuntos
Calcinose/genética , Transtornos Cromossômicos/genética , Transtornos Cromossômicos/patologia , Polimicrogiria/genética , Encefalopatias/genética , Encefalopatias/patologia , Cromossomos Humanos Par 12/genética , Hibridização Genômica Comparativa , Humanos , Lactente , Masculino , Análise em Microsséries
2.
Ann Clin Transl Neurol ; 5(3): 280-296, 2018 03.
Artigo em Inglês | MEDLINE | ID: mdl-29560374

RESUMO

Objective: α (CAMK2A) and ß (CAMK2B) isoforms of Calcium/calmodulin-dependent protein kinase II (CaMKII) play a pivotal role in neuronal plasticity and in learning and memory processes in the brain. Here, we explore the possible involvement of α- and ß-CaMKII variants in neurodevelopmental disorders. Methods: Whole-exome sequencing was performed for 976 individuals with intellectual disability, developmental delay, and epilepsy. The effect of CAMK2A and CAMK2B variants on CaMKII structure and firing of neurons was evaluated by computational structural analysis, immunoblotting, and electrophysiological analysis. Results: We identified a total of five de novo CAMK2A and CAMK2B variants in three and two individuals, respectively. Seizures were common to three individuals with CAMK2A variants. Using a minigene splicing assay, we demonstrated that a splice site variant caused skipping of exon 11 leading to an in-frame deletion of the regulatory segment of CaMKII α. By structural analysis, four missense variants are predicted to impair the interaction between the kinase domain and the regulatory segment responsible for the autoinhibition of its kinase activity. The Thr286/Thr287 phosphorylation as a result of release from autoinhibition was increased in three mutants when the mutants were stably expressed in Neuro-2a neuroblastoma cells. Expression of a CaMKII α mutant in primary hippocampal neurons significantly increased A-type K+ currents, which facilitated spike repolarization of single action potentials. Interpretation: Our data highlight the importance of CaMKII α and CaMKII ß and their autoinhibitory regulation in human brain function, and suggest the enhancement of A-type K+ currents as a possible pathophysiological basis.

3.
Sci Rep ; 7(1): 3552, 2017 06 14.
Artigo em Inglês | MEDLINE | ID: mdl-28615637

RESUMO

Vici syndrome (VICIS) is a rare, autosomal recessive neurodevelopmental disorder with multisystem involvement characterized by agenesis of the corpus callosum, cataracts, cardiomyopathy, combined immunodeficiency, developmental delay, and hypopigmentation. Mutations in EPG5, a gene that encodes a key autophagy regulator, have been shown to cause VICIS, however, the precise pathomechanism underlying VICIS is yet to be clarified. Here, we describe detailed clinical (including brain MRI and muscle biopsy) and genetic features of nine Japanese patients with VICIS. Genetic dissection of these nine patients from seven families identified 14 causative mutations in EPG5. These included five nonsense, two frameshift, three splicing, one missense, and one multi-exon deletion mutations, and two initiation codon variants. Furthermore, cultured skin fibroblasts (SFs) from two affected patients demonstrated partial autophagic dysfunction. To investigate the function of EPG5, siRNA based EPG5 knock-down, and CRISPR/Cas9 mediated EPG5 knock-out HeLa cells were generated. EPG5-depleted cells exhibited a complete block of autophagic flux caused by defective autophagosome-lysosome fusion. Unexpectedly, endocytic degradation was normal in both VICIS SFs and EPG5 depleted cells, suggesting that EPG5 function is limited to the regulation of autophagosome-lysosome fusion.


Assuntos
Agenesia do Corpo Caloso/genética , Agenesia do Corpo Caloso/patologia , Autofagossomos/metabolismo , Catarata/genética , Catarata/patologia , Lisossomos/metabolismo , Transtornos do Neurodesenvolvimento/genética , Transtornos do Neurodesenvolvimento/patologia , Proteínas/genética , Povo Asiático , Proteínas Relacionadas à Autofagia , Biópsia , Encéfalo/diagnóstico por imagem , Encéfalo/patologia , Células Epiteliais/patologia , Saúde da Família , Fibroblastos/patologia , Técnicas de Silenciamento de Genes , Técnicas de Inativação de Genes , Células HeLa , Humanos , Proteínas de Membrana Lisossomal , Imageamento por Ressonância Magnética , Músculos/patologia , Mutação , Proteínas de Transporte Vesicular
4.
Brain Dev ; 39(3): 266-270, 2017 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-27743887

RESUMO

Cerebral folate deficiency due to folate receptor 1 gene (FOLR1) mutations is an autosomal recessive disorder resulting from a brain-specific folate transport defect. It is characterized by late infantile onset, severe psychomotor regression, epilepsy, and leukodystrophy. We describe a consanguineous girl exhibiting severe developmental regression, intractable epilepsy, polyneuropathy, and profound hypomyelination with cortical involvement. Magnetic resonance imaging showed cortical disturbances in addition to profound hypomyelination and cerebellar atrophy. Nerve conduction studies revealed both axonal degeneration and demyelinating features. A diagnosis of cerebral folate deficiency was confirmed by a homozygous c.466T>G (p.W156G) mutation in FOLR1, coupled with extremely low cerebrospinal fluid levels of 5-methyltetrahydrofolate. Her symptoms, neuroradiological findings, and polyneuropathy were alleviated by oral folinic acid treatment in conjunction with intravenous and intramuscular administration therapy. Our patient shows that folinic acid therapy can ameliorate the clinical symptoms, white matter disturbances, cortical insults, and peripheral neuropathy of cerebral folate deficiency caused by FOLR1 mutation. It is important to recognize these clinical symptoms and make a precise diagnosis early on, because cerebral folate deficiency is treatable.


Assuntos
Receptor 1 de Folato/metabolismo , Deficiência de Ácido Fólico/genética , Leucoencefalopatias/genética , Mutação/genética , Doenças do Sistema Nervoso Periférico/genética , Criança , Epilepsia/complicações , Epilepsia/genética , Feminino , Receptor 1 de Folato/deficiência , Deficiência de Ácido Fólico/diagnóstico , Humanos , Leucoencefalopatias/diagnóstico , Leucoencefalopatias/patologia , Imageamento por Ressonância Magnética/métodos , Doenças do Sistema Nervoso Periférico/diagnóstico , Doenças do Sistema Nervoso Periférico/patologia
5.
Brain Dev ; 37(7): 725-8, 2015 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-25480382

RESUMO

We report a case of infantile refractory epilepsy associated with Turner syndrome (TS), showing very frequent, focal clonic seizures of the left upper extremity. Characteristically, in addition to spontaneous fits, her seizure was inducible by rubbing her left hand and forearm for a few seconds. Accordingly, she was diagnosed with a rare form of reflex epilepsy, "rub epilepsy". Neuroradiological investigation indicated the existence of cortical abnormalities, such as focal cortical dysplasia of the right parietal lobe. Patients with TS are reported to have neuroanatomical abnormalities, especially of the parietal lobe. Thus, our case may imply a causal relationship between potential cortical hyperexcitability of the parietal lobe and epilepsy in TS. This is the first reported infantile case of rub epilepsy, and more generally, reflex epilepsy associated with TS.


Assuntos
Encéfalo/patologia , Encéfalo/fisiopatologia , Epilepsia Reflexa/patologia , Epilepsia Reflexa/fisiopatologia , Síndrome de Turner/patologia , Síndrome de Turner/fisiopatologia , Eletroencefalografia , Epilepsia Reflexa/complicações , Feminino , Humanos , Lactente , Imageamento por Ressonância Magnética , Síndrome de Turner/complicações
6.
Brain Dev ; 37(3): 356-8, 2015 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-24856766

RESUMO

Gómez-López-Hernández syndrome (GLHS) is a rare neurocutaneous syndrome characterized by the triad of rhombencephalosynapsis, trigeminal anesthesia, and bilateral parieto-occipital alopecia. We herein describe the first Japanese patient with GLHS characterized by the standard triad with typical craniofacial anomaly including hypertelorism, brachyturricephaly and midface retrusion, and a short stature. This female patient had also exhibited fever-induced convulsive seizures and psychomotor developmental delay since infancy. Brain magnetic resonance imaging showed severe rhombencephalosynapsis, supratentorial abnormalities (aplasia of the septum pellucidum, severe ventricular enlargement, and hypoplasia of the corpus callosum), and hippocampus atrophy. Bilateral ectopic cerebellums were also observed. This report describes the long-term clinical outcome of GLHS and a new neuroradiological finding regarding rhombencephalosynapsis.


Assuntos
Anormalidades Múltiplas/diagnóstico , Alopecia/diagnóstico , Cerebelo/anormalidades , Anormalidades Craniofaciais/diagnóstico , Transtornos do Crescimento/diagnóstico , Síndromes Neurocutâneas/diagnóstico , Anormalidades Múltiplas/patologia , Anormalidades Múltiplas/fisiopatologia , Alopecia/patologia , Alopecia/fisiopatologia , Cerebelo/patologia , Cerebelo/fisiopatologia , Pré-Escolar , Anormalidades Craniofaciais/patologia , Anormalidades Craniofaciais/fisiopatologia , Feminino , Transtornos do Crescimento/patologia , Transtornos do Crescimento/fisiopatologia , Humanos , Japão , Imageamento por Ressonância Magnética , Síndromes Neurocutâneas/patologia , Síndromes Neurocutâneas/fisiopatologia , Rombencéfalo/patologia , Rombencéfalo/fisiopatologia
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