Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndrome.
The syndrome of benign familial infantile convulsions (BFIC) is an autosomal dominant epileptic disorder that is characterized by convulsions, with onset at age 3-12 mo and a favorable outcome. BFIC had been linked to chromosome 19q, whereas the infantile convulsions and choreoathetosis (ICCA) syndr...
Príomhchruthaitheoirí: | Caraballo, R, Pavek, S, Lemainque, A, Gastaldi, M, Echenne, B, Motte, J, Genton, P, Cersósimo, R, Humbertclaude, V, Fejerman, N, Monaco, A, Lathrop, MG, Rochette, J, Szepetowski, P |
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Formáid: | Journal article |
Teanga: | English |
Foilsithe / Cruthaithe: |
2001
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Míreanna comhchosúla
Míreanna comhchosúla
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Infantile benign convulsions and choreoathetosis: the ICCA syndrome
de réir: Rochette, J, et al.
Foilsithe / Cruthaithe: (1997) -
Linkage of benign familial infantile convulsions to the ICCA region on chromosome 16.
de réir: Szepetowski, P, et al.
Foilsithe / Cruthaithe: (2000) -
Familial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16.
de réir: Szepetowski, P, et al.
Foilsithe / Cruthaithe: (1997) -
Familiar infantile convulsions and paroxysmal choreoathetosis (ICCA): a new neurological syndrome linked to the pericentromeric region of human chromosome 16.
de réir: Szepetowski, P, et al.
Foilsithe / Cruthaithe: (1997) -
Association of infantile convulsions with paroxysmal dyskinesias (ICCA syndrome): confirmation of linkage to human chromosome 16p12-q12 in a Chinese family.
de réir: Lee, W, et al.
Foilsithe / Cruthaithe: (1998)