Epilepsy and Mental Retardation limited to Females (EFMR) which links to Xq22 has been reported in only one family. We aimed to determine if there was a distinctive phenotype that would enhance recognition of this disorder. We ascertained four unrelated families (two Australian, two Israeli) where seizures in females were transmitted through carrier males. Detailed clinical assessment was performed on 58 individuals, using a validated seizure questionnaire, neurological examination and review of EEG and imaging studies. Gene localization was examined using Xq22 microsatellite markers. Twenty-seven affected females had a mean seizure onset of 14 months (range 6-36) typically presenting with convulsions. All had convulsive attacks at some sta...
BACKGROUND: Eight different deletions and point variants of the X-chromosomal gene CNKSR2 have been ...
Item does not contain fulltextOBJECTIVE: IQSEC2 is an X-linked gene associated with intellectual dis...
Summary: Background: Familial partial epilepsy with variable foci (FPEVF) is an autosomal dominant s...
Epilepsy and Mental Retardation limited to Females (EFMR) which links to Xq22 has been reported in o...
Epilepsy and Mental Retardation limited to Females (EFMR) which links to Xq22 has been reported in o...
Background: Epilepsy and mental retardation limited to females (EFMR) is an intriguing X-linked diso...
Epilepsy and mental retardation limited to females (EFMR) is a genetic disorder that affects females...
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/66148/1/j.1399-0004.1990.tb03594.x.pd
Purpose Pathogenic variants in the X-linked gene NEXMIF (previously KIAA2022) are associated with in...
Epilepsy and abnormal electroencephalographic (EEG) patterns have been reported in mentally retarded...
Purpose Pathogenic variants in the X-linked gene NEXMIF (previously KIAA2022) are associated with in...
Epilepsy and Mental Retardation Limited to Females (EFMR) is an infantile onset disorder characteriz...
Epilepsy and mental retardation limited to females (EFMR) is an intriguing X-linked disorder, which ...
The IQSEC2- related disorders represent a spectrum of X-chromosome phenotypes with intellectual disa...
BACKGROUND: Mutations in the KIAA2022 gene have been reported in male patients with X-linked intelle...
BACKGROUND: Eight different deletions and point variants of the X-chromosomal gene CNKSR2 have been ...
Item does not contain fulltextOBJECTIVE: IQSEC2 is an X-linked gene associated with intellectual dis...
Summary: Background: Familial partial epilepsy with variable foci (FPEVF) is an autosomal dominant s...
Epilepsy and Mental Retardation limited to Females (EFMR) which links to Xq22 has been reported in o...
Epilepsy and Mental Retardation limited to Females (EFMR) which links to Xq22 has been reported in o...
Background: Epilepsy and mental retardation limited to females (EFMR) is an intriguing X-linked diso...
Epilepsy and mental retardation limited to females (EFMR) is a genetic disorder that affects females...
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/66148/1/j.1399-0004.1990.tb03594.x.pd
Purpose Pathogenic variants in the X-linked gene NEXMIF (previously KIAA2022) are associated with in...
Epilepsy and abnormal electroencephalographic (EEG) patterns have been reported in mentally retarded...
Purpose Pathogenic variants in the X-linked gene NEXMIF (previously KIAA2022) are associated with in...
Epilepsy and Mental Retardation Limited to Females (EFMR) is an infantile onset disorder characteriz...
Epilepsy and mental retardation limited to females (EFMR) is an intriguing X-linked disorder, which ...
The IQSEC2- related disorders represent a spectrum of X-chromosome phenotypes with intellectual disa...
BACKGROUND: Mutations in the KIAA2022 gene have been reported in male patients with X-linked intelle...
BACKGROUND: Eight different deletions and point variants of the X-chromosomal gene CNKSR2 have been ...
Item does not contain fulltextOBJECTIVE: IQSEC2 is an X-linked gene associated with intellectual dis...
Summary: Background: Familial partial epilepsy with variable foci (FPEVF) is an autosomal dominant s...