BACKGROUND: The unequivocal diagnosis of fragile Xq syndrome is based in the direct analysis of the underlying FMR-1 gene mutation, that consists in an increased number of trinucleotide CGG repetitions. AIM: To study families with fragile Xq syndrome, using the Southern technique for the analysis of the mutation. SUBJECTS AND METHODS: Fifteen individuals, pertaining to 6 families with fragile Xq syndrome, were studied. Clinical, cytogenetic and molecular analysis using Southern technique, were done. RESULTS: Five male individuals had a clinically evident syndrome, confirmed by cytogenetic analysis that showed fragility in 10 to 29% of studied cells. One subject with a clinical picture suggesting fragile Xq had a normal cytogenetic study. The other studied subjects were the mothers of the five subjects with the syndrome, that must be carriers, and four brothers. Molecular analysis showed that seven subjects (5 males) had a complete mutation, five (4 females) were carriers of a pre mutation and three (2 males) did not have the mutation. CONCLUSIONS: The Southern technique allows to verify the normal condition of FRAXA locus, identify carriers and to detect complete mutations in fragile Xq syndrome.
BACKGROUND: The unequivocal diagnosis of fragile Xq syndrome is based in the direct analysis of the underlying FMR-1 gene mutation, that consists in an increased number of trinucleotide CGG repetitions. AIM: To study families with fragile Xq syndrome, using the Southern technique for the analysis of the mutation. SUBJECTS AND METHODS: Fifteen individuals, pertaining to 6 families with fragile Xq syndrome, were studied. Clinical, cytogenetic and molecular analysis using Southern technique, were done. RESULTS: Five male individuals had a clinically evident syndrome, confirmed by cytogenetic analysis that showed fragility in 10 to 29% of studied cells. One subject with a clinical picture suggesting fragile Xq had a normal cytogenetic study. The other studied subjects were the mothers of the five subjects with the syndrome, that must be carriers, and four brothers. Molecular analysis showed that seven subjects (5 males) had a complete mutation, five (4 females) were carriers of a pre mutation and three (2 males) did not have the mutation. CONCLUSIONS: The Southern technique allows to verify the normal condition of FRAXA locus, identify carriers and to detect complete mutations in fragile Xq syndrome.
Authors: David J Amor; David E Godler; Emma K Baker; Marta Arpone; Solange M Aliaga; Lesley Bretherton; Claudine M Kraan; Minh Bui; Howard R Slater; Ling Ling; David Francis; Matthew F Hunter; Justine Elliott; Carolyn Rogers; Michael Field; Jonathan Cohen; Kim Cornish; Lorena Santa Maria; Victor Faundes; Bianca Curotto; Paulina Morales; Cesar Trigo; Isabel Salas; Angelica M Alliende Journal: Mol Autism Date: 2019-05-03 Impact factor: 7.509
Authors: Emma K Baker; Marta Arpone; Solange Aliaga Vera; Lesley Bretherton; Alexandra Ure; Claudine M Kraan; Minh Bui; Ling Ling; David Francis; Matthew F Hunter; Justine Elliott; Carolyn Rogers; Michael J Field; Jonathan Cohen; Lorena Santa Maria; Victor Faundes; Bianca Curotto; Paulina Morales; Cesar Trigo; Isabel Salas; Angelica M Alliende; David J Amor; David E Godler Journal: J Neurodev Disord Date: 2019-12-26 Impact factor: 4.025
Authors: David J Amor; David E Godler; Emma K Baker; Marta Arpone; Claudine Kraan; Minh Bui; Carolyn Rogers; Michael Field; Lesley Bretherton; Ling Ling; Alexandra Ure; Jonathan Cohen; Matthew F Hunter; Lorena Santa María; Victor Faundes; Bianca Curotto; Paulina Morales; Cesar Trigo; Isabel Salas; Angelica Alliende Journal: Sci Rep Date: 2020-07-16 Impact factor: 4.379