Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12104/44279
Title: Ring-20-syndrome and loss of telomeric regions
Author: Garcia-Cruz, D.
Isabel Vasquez, A.
Perez-Rulfo, D.
Omayra Davalos, N.
Manuel Penaloza, J.
Elias Garcia-Ortiz, J.
Patino-Garcia, B.
Sanchez-Corona, J.
Issue Date: 2000
Abstract: A patient aged 10 years and 8 months with a ring-20-syndrome was studied. Clinically he presented normal psychomotor development until 25 months of age when he began with right simple partial motor seizures. He presented minimal dysmorphism, generalized tonic-clonic seizures refractory to medical therapy and behavioral troubles. He was submitted to a callosotomy when he presented an electric status, subsequently, he was treated with anticonvulsivants and felbamate and the seizures were controlled. The karyotype showed a chromosomal complement 46,XY,r(20)(p13q13.3) with loss of the telomeric regions evidenced by FISH. The mother had normal karyotype. The clinical and cytogenetic features of previous cases described in the literature were compared leading to a better characterization of this syndrome. 2000 Editions scientifiques et medicales Elsevier SAS.
URI: http://www.scopus.com/inward/record.url?eid=2-s2.0-0034519833&partnerID=40&md5=693668be759421f052fb7b9b3fbc954e
http://hdl.handle.net/20.500.12104/44279
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