Multi-institutional study on the correlation between chromosomal abnormalities and epilepsy.

@article{Kumada2005MultiinstitutionalSO,
  title={Multi-institutional study on the correlation between chromosomal abnormalities and epilepsy.},
  author={Tomohiro Kumada and Masatoshi Ito and Tomoko Miyajima and Tatsuya Fujii and Takehiko Okuno and Toshin Go and Haruo Hattori and Mieko Yoshioka and Ken-ichiro Kobayashi and Osamu Kanazawa and Jun Tohyama and Noriyuki Akasaka and Takanori Kamimura and Mutsuo Sasagawa and Hideki Amagane and Kozo Mutoh and Yuriko Yamori and Toyoko Kanda and Naoko Yoshida and Haruyo Hirota and Rieko Tanaka and Yasushi Hamada},
  journal={Brain & development},
  year={2005},
  volume={27 2},
  pages={127-34}
}
While there is an abundance of literature describing the association of chromosome aberrations with epilepsy, only a few refer to the detailed features of epilepsy. It is important to investigate the associations between specific chromosome abnormalities and features of epilepsy to identify genes involved in epilepsy and treat them more effectively. We investigated the correlation between specific chromosome aberrations and epilepsy by sending questionnaires to the members of Kyoto Multi… CONTINUE READING

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Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In 4p- syndrome , febrile seizures were often seen , and unilateral or generalized clonic or tonic - clonic status epilepticus were characteristic .
In 4p- syndrome , febrile seizures were often seen , and unilateral or generalized clonic or tonic - clonic status epilepticus were characteristic .
In 4p- syndrome , febrile seizures were often seen , and unilateral or generalized clonic or tonic - clonic status epilepticus were characteristic .
In 4p- syndrome , febrile seizures were often seen , and unilateral or generalized clonic or tonic - clonic status epilepticus were characteristic .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
In Down syndrome , West syndrome and focal epilepsy were common and the prognosis of epilepsy in West syndrome with Down syndrome was good .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
EpilepsyIs related toSeizures
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
EpilepsyParent is nichdWest Syndrome
In Down syndrome , West syndrome and focal epilepsy were common and the prognosis of epilepsy in West syndrome with Down syndrome was good .
In Down syndrome , West syndrome and focal epilepsy were common and the prognosis of epilepsy in West syndrome with Down syndrome was good .
In Down syndrome , West syndrome and focal epilepsy were common and the prognosis of epilepsy in West syndrome with Down syndrome was good .
In Down syndrome , West syndrome and focal epilepsy were common and the prognosis of epilepsy in West syndrome with Down syndrome was good .
In Down syndrome , West syndrome and focal epilepsy were common and the prognosis of epilepsy in West syndrome with Down syndrome was good .
In Down syndrome , West syndrome and focal epilepsy were common and the prognosis of epilepsy in West syndrome with Down syndrome was good .
In Down syndrome , West syndrome and focal epilepsy were common and the prognosis of epilepsy in West syndrome with Down syndrome was good .
In Down syndrome , West syndrome and focal epilepsy were common and the prognosis of epilepsy in West syndrome with Down syndrome was good .
In Down syndrome , West syndrome and focal epilepsy were common and the prognosis of epilepsy in West syndrome with Down syndrome was good .
In Down syndrome , West syndrome and focal epilepsy were common and the prognosis of epilepsy in West syndrome with Down syndrome was good .
In Down syndrome , West syndrome and focal epilepsy were common and the prognosis of epilepsy in West syndrome with Down syndrome was good .
In Down syndrome , West syndrome and focal epilepsy were common and the prognosis of epilepsy in West syndrome with Down syndrome was good .
In Down syndrome , West syndrome and focal epilepsy were common and the prognosis of epilepsy in West syndrome with Down syndrome was good .
In Down syndrome , West syndrome and focal epilepsy were common and the prognosis of epilepsy in West syndrome with Down syndrome was good .
FeverNo subtypeSeizures
In 4p- syndrome , febrile seizures were often seen , and unilateral or generalized clonic or tonic - clonic status epilepticus were characteristic .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
SeizuresNo subtypeFever
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In 4p- syndrome , febrile seizures were often seen , and unilateral or generalized clonic or tonic - clonic status epilepticus were characteristic .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
SeizuresIs related toEpilepsy
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
SeizuresMapped fromEpilepsy
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In Angelman and Prader - Willi syndromes , febrile seizures occurred frequently , the onset of epilepsy was in early childhood and seizure phenotype was multiple .
In 4p- syndrome , febrile seizures were often seen , and unilateral or generalized clonic or tonic - clonic status epilepticus were characteristic .
In 4p- syndrome , febrile seizures were often seen , and unilateral or generalized clonic or tonic - clonic status epilepticus were characteristic .
In 4p- syndrome , febrile seizures were often seen , and unilateral or generalized clonic or tonic - clonic status epilepticus were characteristic .
In 4p- syndrome , febrile seizures were often seen , and unilateral or generalized clonic or tonic - clonic status epilepticus were characteristic .
In 4p- syndrome , febrile seizures were often seen , and unilateral or generalized clonic or tonic - clonic status epilepticus were characteristic .
In Down syndrome , West syndrome and focal epilepsy were common and the prognosis of epilepsy in West syndrome with Down syndrome was good .
In Down syndrome , West syndrome and focal epilepsy were common and the prognosis of epilepsy in West syndrome with Down syndrome was good .
In Down syndrome , West syndrome and focal epilepsy were common and the prognosis of epilepsy in West syndrome with Down syndrome was good .
In Down syndrome , West syndrome and focal epilepsy were common and the prognosis of epilepsy in West syndrome with Down syndrome was good .
In 4p- syndrome , febrile seizures were often seen , and unilateral or generalized clonic or tonic - clonic status epilepticus were characteristic .
In 4p- syndrome , febrile seizures were often seen , and unilateral or generalized clonic or tonic - clonic status epilepticus were characteristic .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
Chromosome abnormalities included : Down syndrome ( n = 19 ) ; Angelman syndrome ( n = 8) ; Prader - Willi syndrome ( n = 4 ) ; 4p- syndrome ( n = 3 ) ; 1q- syndrome ( n = 2 ) ; 5p- syndrome ( n = 2 ) ; Miller - Dieker syndrome ( n = 2 ) ; 18q- syndrome ; ( n = 2 ) ; Klinefelter syndrome ; ( n = 2 ) ; and 32 other individual chromosomal aberrations .
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