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CRKL Gene Deletion in Familial Zinner (OSVIRA) and OHVIRA Syndromes
PediatricsWe present the first description of a family in which 2 siblings show alternative expression of CRKL gene deletion as the phenotypes of Zinner (OSVIRA, obstructed seminal vesicle and ipsilateral renal agenesis) and OHVIRA (obstructed hemivagina with an ipsilateral renal anomaly) syndromes.
Hannah L, Rhodes +3 more
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Herlyn-Werner-Wunderlich syndrome- OHVIRA syndrome: a rare congenital anomaly
2016Clinical History Image Findings Discussion Find Diagnosis Differential ...
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Atypical OHVIRA syndrome: cases of chronic discharge
Journal of Pediatric and Adolescent Gynecology, 2022Kristina Arion, Nancy Van Eyk
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Challenges in Diagnosis of Ohvira Syndrome
Journal of Pediatric and Adolescent Gynecology, 2016Carolyn Haunschild +2 more
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OHVIRA syndrome: A mystery of female pelvis
Learning objectives Background Findings and procedure details Conclusion Personal information and conflict of interest ...openaire +1 more source
Diverse Presentations of OHVIRA Syndrome: A Case Series
Clinical Pediatrics, 2020Swati Jha, Shahram Abdi
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A case of OHVIRA / Herlyn–Werner–Wunderlich syndrome
Clinical History: A 13-year-old female came with complaints of a slowly growing suprapubic mass since a few months and lower abdominal discomfort. She was further advised to undergo ultrasound imaging and subsequently CT abdomen for renal anomaly, and MRI pelvis for further evaluation.openaire +1 more source
True Management of Herlyn-Werner-Wunderlich Syndrome (OHVIRA Syndrome)
Journal of Minimally Invasive Gynecology, 2016C Atabekoglu +4 more
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