Cytogenetic and molecular screening of the daz gene family in a population of infertile males
The purpose of this study was to evalúate the frequency of Y chromosome structural, numerical, chromosomal and genetic abnormalities, as well as DAZ gene microdeletions in the Y chromosome in a population of infertile males. Genetic abnormalities have been established to date in up to 24% of males h...
- Autores:
-
Ruiz Suárez, Nubia Amparo
Godoy Silva, Henry
Giraldo, Alejandro
Aristizábal Gutiérrez, Fabio Ancízar
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2003
- Institución:
- Universidad Nacional de Colombia
- Repositorio:
- Universidad Nacional de Colombia
- Idioma:
- spa
- OAI Identifier:
- oai:repositorio.unal.edu.co:unal/22189
- Acceso en línea:
- https://repositorio.unal.edu.co/handle/unal/22189
http://bdigital.unal.edu.co/13223/
- Palabra clave:
- azoospermia
oligozoospermia
microdeleciones
ICSI
azoospermia
oligozoospermia
microdeletions
ICSI
- Rights
- closedAccess
- License
- Atribución-NoComercial 4.0 Internacional
Summary: | The purpose of this study was to evalúate the frequency of Y chromosome structural, numerical, chromosomal and genetic abnormalities, as well as DAZ gene microdeletions in the Y chromosome in a population of infertile males. Genetic abnormalities have been established to date in up to 24% of males having severe abnormalities in their sperm (Dohle et al. 2002); deletion of the DAZ gene family (deleted in azoospermia) is the most common cause. It has been found in 6% of the oligozoospermias and in 12% of the azoospermias (Van Landuyt et al. 2000). A population of 20 azoospermic and 10 oligozoospermic males was studied. Five males having normal sperm parameters were used as controls. Each sample was karyotyped (QFQ banding) and underwent sY254, sY255 and sY257 molecular amplification. Genetic study revealed alterations in 16.6% of the cases: 6.6% at chromosome level and 10% at molecule level. No chromosomal or molecular gene alterations were detected in control males. The frequencies found lead to a broader population-based study being recommended. They confirmed the need for performing judicious genetic counselling in infertile couples with male factor infertility to avoid or minimise the risks of trans-mitting these abnormalities to offspring and provide better prognosis for assisted reproductive techniques in such patients. Key words: azoospermia; oligozoospermia; microdeletions; ICSI |
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