Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/32577
Title: Genetic screening of infertile men.
Authors: Lynch M.;Salvado C.;McLachlan R.I.;de Krester D.M.;Cram D.;O'Bryan M.K.
Institution: (Cram, O'Bryan, Salvado, de Krester) Monash Inst. of Reprod./Development, Monash University, 27-31 Wright St., Clayton, Vic., Australia (Cram) Monash IVF, Epworth Hospital, Melbourne, Vic., Australia (Lynch, McLachlan) Prince Henry's Inst. Reprod./Devmt., Department of Obstetrics/Gynaecology, Monash Medical Centre, Melbourne, Vic., Australia
Issue Date: 18-Oct-2012
Copyright year: 2004
Publisher: CSIRO (P.O. Box 1139, Collingwood VIC 3066, Australia)
Place of publication: Australia
Publication information: Reproduction, Fertility and Development. 16 (5) (pp 573-580), 2004. Date of Publication: 2004.
Abstract: Male infertility is an extraordinarily common medical condition, affecting 1 in 20 men. According to the World Health Organization, this condition is now considered to be a complex disease involving physical, genetic and environmental factors. With continuing advances in our understanding of male reproductive physiology and endocrinology, together with the availability of the complete sequence of the human genome and powerful functional genomic techniques, the stage is now set to identify the genes that are essential for spermatogenesis. Given that the process of spermatogenesis, from the germ cell to mature sperm, is complex, the challenge for research is to develop the strategies for identifying new genetic causes of idiopathic male infertility and defining genotypes associated with specific defects in semen parameters and testicular pathologies. Such information will form the basis of new genetic tests that will allow the clinician to make an accurate diagnosis of the male partner and a more informed decision about treatment options for the couple. © CSIRO 2004.
DOI: http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1071/RD03097
PubMed URL: 15367372 [http://www.ncbi.nlm.nih.gov/pubmed/?term=15367372]
ISSN: 1031-3613
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/32577
Type: Article
Subjects: *genetic screening
genotype
germ cell
human
intracytoplasmic sperm injection
male
*male infertility/di [Diagnosis]
*male infertility/et [Etiology]
*male infertility/th [Therapy]
medical information
outcomes research
pathogenesis
semen analysis
spermatogenesis
spermatozoon maturation
testis disease
treatment planning
genomic DNA/ec [Endogenous Compound]
membrane protein/ec [Endogenous Compound]
messenger RNA/ec [Endogenous Compound]
protein Ret/ec [Endogenous Compound]
transmembrane conductance regulator/ec [Endogenous Compound]
human genome
article
autosomal recessive inheritance
azoospermia/di [Diagnosis]
azoospermia/et [Etiology]
azoospermia/th [Therapy]
chromosome deletion
chromosome Yq
cystic fibrosis
diagnostic accuracy
DNA determination
environmental factor
gene function
gene identification
gene mutation
gene sequence
gene technology
genetic analysis
genetic association
gene mutation
gene sequence
gene technology
genetic analysis
genetic association
*genetic screening
genotype
germ cell
human
human genome
intracytoplasmic sperm injection
male
*male infertility / *diagnosis / *etiology / *therapy
medical information
outcomes research
pathogenesis
semen analysis
spermatogenesis
azoospermia / diagnosis / etiology / therapy
testis disease
treatment planning
autosomal recessive inheritance
article
spermatozoon maturation
chromosome deletion
chromosome Yq
cystic fibrosis
diagnostic accuracy
DNA determination
environmental factor
gene function
gene identification
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