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
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Cariotipagem
Limite:
Female
/
Humans
Idioma:
En
Revista:
Arch. Iran. Med.
Ano de publicação:
2000