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Published in 2021 at "Annals of Medicine and Surgery"
DOI: 10.1016/j.amsu.2021.102449
Abstract: Introduction and importance Congenital unilateral absence of the vas deferens and ipsilateral renal agenesis is a rare condition in which the vas deferens is absent unilateral due to a congenital anomaly. This report illustrates the…
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Keywords:
absence;
vas deferens;
unilateral absence;
congenital unilateral ... See more keywords
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Published in 2018 at "Andrologia"
DOI: 10.1111/and.12994
Abstract: Congenital absence of the vas deferens (CAVD) is a relatively rare anomaly that may contribute to male infertility. The aim of this study was to evaluate the clinical features of patients with CAVD and to…
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Keywords:
comorbidity congenital;
congenital absence;
absence vas;
vas deferens ... See more keywords
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Published in 2019 at "Andrology"
DOI: 10.1111/andr.12592
Abstract: Congenital absence of vas deferens (CAVD) is a major cause of obstructive azoospermia. Mutations in CFTR and ADGRG2 are responsible for this disease. However, until now the genetic spectrum of the CFTR and ADGRG2 genes…
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Keywords:
congenital absence;
vas deferens;
genetic spectrum;
absence vas ... See more keywords
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Published in 2020 at "Frontiers in Genetics"
DOI: 10.3389/fgene.2020.00104
Abstract: Background Apert, Pfeiffer, and Crouzon syndromes are autosomal dominant diseases characterized by craniosynostosis. They are paternal age effect disorders. The association between paternal age and Beare–Stevenson syndrome (BSS), a very rare and severe craniosynostosis, is…
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Keywords:
beare stevenson;
bilateral absence;
age;
congenital bilateral ... See more keywords
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Published in 2022 at "Frontiers in Genetics"
DOI: 10.3389/fgene.2022.1035468
Abstract: Congenital absence of the vas deferens (CAVD) is a major cause of obstructive azoospermia. Mutations of CFTR and ADGRG2 cause the majority of CAVD. Despite this, 10%–20% of CAVD patients remain without a clear genetic…
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Keywords:
vas deferens;
absence vas;
congenital absence;
cavd ... See more keywords
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1
Published in 2019 at "Asian Journal of Andrology"
DOI: 10.4103/aja.aja_112_18
Abstract: including physical examination, rectal ultrasound examination, and basal hormonal examination. Consequently, aside from the absence of bilateral vas deferens and an elevated sweat chloride concentration (213.50 mmol l−1) detected only in the patient (Figure 1a…
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Keywords:
gene;
cbavd;
absence vas;
vas deferens ... See more keywords
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Published in 2022 at "Asian Journal of Andrology"
DOI: 10.4103/aja20225
Abstract: Patients with congenital unilateral absence of the vas deferens (CUAVD) manifest diverse symptoms from normospermia to azoospermia. Treatment for CUAVD patients with obstructive azoospermia (OA) is complicated, and there is a lack of relevant reports.…
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Keywords:
unilateral absence;
vas deferens;
absence vas;
congenital unilateral ... See more keywords
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Published in 2020 at "Urology Annals"
DOI: 10.4103/ua.ua_155_18
Abstract: We present a case report of a 25-year-old obese man complaining of primary infertility for 2 years. After a thorough examination and investigation were done, he had congenital unilateral absence of vas deferens with ipsilateral…
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Keywords:
vas deferens;
absence vas;
congenital unilateral;
vas ... See more keywords
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Published in 2018 at "Clinical and Experimental Reproductive Medicine"
DOI: 10.5653/cerm.2018.45.1.48
Abstract: We report the case of a 46-year-old Chinese male patient who visited our clinic complaining of infertility. Semen analysis revealed azoospermia, and azoospermia factor c region partial deletion (b1/b3) was detected using Y chromosome microdeletion…
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Keywords:
spermatogenesis;
vas deferens;
bilateral absence;
deletion ... See more keywords