AbstractWe report two individual cases of cardio-facio-cutaneous (CFC) syndrome with severe neurological impairment consisting of infantile spasms with hypsarrhythmia and refractory epilepsy with multifocal epileptic paroxysms such as modified hypsarrhythmia. Both cases shared diffuse brain atrophy and severely delayed myelination on neuroimaging. Genetic analysis revealed individual heterozygous mutations in the KRAS (phenotype of CFC/Noonan syndrome) and BRAF genes (phenotype of CFC syndrome). Neurological impairment in cases with mutations in the RAS/MAPK (mitogen activated protein kinase) signal pathway may be more severe, and could be linked to some forms of refractory epilepsy, especially epileptic encephalopathy that includes infanti...
The RAS-MAPK syndromes are a group of clinically and genetically related disorders, characterized by...
Background: Microcephaly-capillary malformation (MIC-CAP) syndrome is a newly described autosomal re...
Background: Mutations in the KCTD7 gene have been associated with progressive myoclonus epilepsy and...
AbstractWe report two individual cases of cardio-facio-cutaneous (CFC) syndrome with severe neurolog...
Gene variants that dysregulate signaling through the RAS-MAPK pathway cause cardiofaciocutaneous syn...
Cardiofaciocutaneous syndrome (CFCS) is a rare developmental disorder caused by upregulated signalin...
Background: Cardio-facio-cutaneous syndrome (CFCS) belongs to RASopathies, a group of conditions cau...
Aim: Epilepsy is commonly observed in congenital disorders of glycosylation (CDG), but no distinctiv...
This report illustrates the difficulties in diagnosing complex cases and demonstrates how whole exom...
Sebaceous nevus syndrome is a neurocutaneous disorder that shows neurological symptoms such as epile...
Congenital disorders of glycosylation (CDG) are a group of rare metabolic diseases, characterized by...
Cardio-facio-cutaneous (CFC) syndrome is a very rare and sporadic disease whose characteristics incl...
Cardio-facio-cutaenous (CFC) syndrome is a developmental disorder causing mental retardation and mul...
Pontocerebellar hypoplasia is a group of heterogeneous neurodevelopmental disorders characterized by...
Introduction: Cortical dysplasia carries significant morbidities such as seizures and delayed milest...
The RAS-MAPK syndromes are a group of clinically and genetically related disorders, characterized by...
Background: Microcephaly-capillary malformation (MIC-CAP) syndrome is a newly described autosomal re...
Background: Mutations in the KCTD7 gene have been associated with progressive myoclonus epilepsy and...
AbstractWe report two individual cases of cardio-facio-cutaneous (CFC) syndrome with severe neurolog...
Gene variants that dysregulate signaling through the RAS-MAPK pathway cause cardiofaciocutaneous syn...
Cardiofaciocutaneous syndrome (CFCS) is a rare developmental disorder caused by upregulated signalin...
Background: Cardio-facio-cutaneous syndrome (CFCS) belongs to RASopathies, a group of conditions cau...
Aim: Epilepsy is commonly observed in congenital disorders of glycosylation (CDG), but no distinctiv...
This report illustrates the difficulties in diagnosing complex cases and demonstrates how whole exom...
Sebaceous nevus syndrome is a neurocutaneous disorder that shows neurological symptoms such as epile...
Congenital disorders of glycosylation (CDG) are a group of rare metabolic diseases, characterized by...
Cardio-facio-cutaneous (CFC) syndrome is a very rare and sporadic disease whose characteristics incl...
Cardio-facio-cutaenous (CFC) syndrome is a developmental disorder causing mental retardation and mul...
Pontocerebellar hypoplasia is a group of heterogeneous neurodevelopmental disorders characterized by...
Introduction: Cortical dysplasia carries significant morbidities such as seizures and delayed milest...
The RAS-MAPK syndromes are a group of clinically and genetically related disorders, characterized by...
Background: Microcephaly-capillary malformation (MIC-CAP) syndrome is a newly described autosomal re...
Background: Mutations in the KCTD7 gene have been associated with progressive myoclonus epilepsy and...