Articles with "absence vas" as a keyword



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Congenital unilateral absence of the vas deferens with ipsilateral renal agenesis encountered during laparoscopic totally extraperitoneal inguinal hernia repair in an adult patient: A case report

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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… read more here.

Keywords: absence; vas deferens; unilateral absence; congenital unilateral ... See more keywords
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Comorbidity of the congenital absence of the vas deferens

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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… read more here.

Keywords: comorbidity congenital; congenital absence; absence vas; vas deferens ... See more keywords
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Expanding the phenotypic and genetic spectrum of Chinese patients with congenital absence of vas deferens bearing CFTR and ADGRG2 alleles

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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… read more here.

Keywords: congenital absence; vas deferens; genetic spectrum; absence vas ... See more keywords
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Report of a Father With Congenital Bilateral Absence of the Vas Deferens Fathering a Child With Beare–Stevenson Syndrome

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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… read more here.

Keywords: beare stevenson; bilateral absence; age; congenital bilateral ... See more keywords
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Congenital absence of the vas deferens with hypospadias or without hypospadias: Phenotypic findings and genetic considerations

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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… read more here.

Keywords: vas deferens; absence vas; congenital absence; cavd ... See more keywords
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SCNN1B and CA12 play vital roles in occurrence of congenital bilateral absence of vas deferens (CBAVD)

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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… read more here.

Keywords: gene; cbavd; absence vas; vas deferens ... See more keywords
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Clinical features and microsurgical reconstruction of congenital unilateral absence of the vas deferens with obstructive azoospermia: a tertiary care center experience

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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.… read more here.

Keywords: unilateral absence; vas deferens; absence vas; congenital unilateral ... See more keywords
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Congenital unilateral absence of vas deferens with contralateral testicular atrophy

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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… read more here.

Keywords: vas deferens; absence vas; congenital unilateral; vas ... See more keywords
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An infertile patient with Y chromosome b1/b3 deletion presenting with congenital bilateral absence of the vas deferens with normal spermatogenesis

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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… read more here.

Keywords: spermatogenesis; vas deferens; bilateral absence; deletion ... See more keywords