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Archives of Iranian Medicine. 2000; 3 (3): 151-3
em En | IMEMR | ID: emr-53433
Biblioteca responsável: EMRO
Robertsonian translocation is one of the major chromosomal re-arrangements and comprises 18% of total genetic abnormalities. It occurs between different chromosomes and chromosomal segments and less than 0.2% of individuals carry a symptomatic chromosomal rearrangement. However, the t[22;22]is a rare phenomenon which mainly manifests as familial monosomy or trisomy. We report on a 30-year old woman who was referred to a pathological laboratory in Kerman, Iran. She had no mental retardation, but suffered from repeated abortions. On the basis of GTG-banding and karyotyping, it was found that a Robertsonian translocation in the chromosome 22;22 was the primary cause of this syndrome
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Índice: IMEMR Assunto principal: Translocação Genética / Cromossomos Humanos Par 22 / Aberrações Cromossômicas / Cariotipagem Limite: Female / Humans Idioma: En Revista: Arch. Iran. Med. Ano de publicação: 2000
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Índice: IMEMR Assunto principal: Translocação Genética / Cromossomos Humanos Par 22 / Aberrações Cromossômicas / Cariotipagem Limite: Female / Humans Idioma: En Revista: Arch. Iran. Med. Ano de publicação: 2000