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Molecular Pathology of Cryptorchidism-Induced Infertility
- Source :
- Sexual Development. 9:269-278
- Publication Year :
- 2015
- Publisher :
- S. Karger AG, 2015.
-
Abstract
- Cryptorchidism is the most common cause of non-obstructive azoospermia in man. In contrast to the general belief that temperature-dependent effects on the undescended gonad damage cryptorchid testes before sexual maturation is complete, molecular pathology strongly supports the theory that impaired mini-puberty is responsible for azoospermia and infertility in cryptorchidism. Molecular biological observations favor LH deficiency, with EGR4 as a master regulatory gene in Leydig cell dysgenesis, as the reason for impaired mini-puberty, and recent evidence supports the idea that infertility in cryptorchidism is a consequence of alterations in the Piwi pathway.
- Subjects :
- Male
Infertility
endocrine system
Embryology
medicine.medical_specialty
Gonad
Endocrinology, Diabetes and Metabolism
Piwi-interacting RNA
Biology
Male infertility
Dysgenesis
Internal medicine
Cryptorchidism
medicine
Humans
Testosterone
Infertility, Male
Azoospermia
Leydig cell
urogenital system
Molecular pathology
Puberty
Leydig Cells
Luteinizing Hormone
medicine.disease
medicine.anatomical_structure
Endocrinology
Argonaute Proteins
Early Growth Response Transcription Factors
Mutation
Developmental Biology
Subjects
Details
- ISSN :
- 16615433 and 16615425
- Volume :
- 9
- Database :
- OpenAIRE
- Journal :
- Sexual Development
- Accession number :
- edsair.doi.dedup.....31875f63d327fe40900faaa4361ecaf0
- Full Text :
- https://doi.org/10.1159/000442059