Uma malformação rara da vagina, caracterizada pela presença de uma espécie de "parede" (septo) transversal, que pode ser completa ou incompleta, em qualquer ponto da vagina (mas geralmente na parte de cima ou no meio). Isso acontece por uma falha na união completa de duas partes que formam a vagina durante o desenvolvimento do bebê no útero. Essa condição raramente é diagnosticada em recém-nascidos ou bebês, a não ser que cause um acúmulo grande de muco e líquido na vagina (hidromucocolpos). Quando a parede é completa, os sintomas podem incluir: ausência de menstruação (amenorreia primária), dor na pelve que se repete mensalmente, dor durante a relação sexual (dispareunia), ou uma "massa" (inchaço) na pelve causada por acúmulo de sangue menstrual. Já quando a parede é incompleta, pode causar dor durante a relação sexual e cólicas menstruais fortes (dismenorreia).
Introdução
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Uma malformação rara da vagina, caracterizada pela presença de uma espécie de "parede" (septo) transversal, que pode ser completa ou incompleta, em qualquer ponto da vagina (mas geralmente na parte de cima ou no meio). Isso acontece por uma falha na união completa de duas partes que formam a vagina durante o desenvolvimento do bebê no útero. Essa condição raramente é diagnosticada em recém-nascidos ou bebês, a não ser que cause um acúmulo grande de muco e líquido na vagina (hidromucocolpos). Quando a parede é completa, os sintomas podem incluir: ausência de menstruação (amenorreia primária), dor na pelve que se repete mensalmente, dor durante a relação sexual (dispareunia), ou uma "massa" (inchaço) na pelve causada por acúmulo de sangue menstrual. Já quando a parede é incompleta, pode causar dor durante a relação sexual e cólicas menstruais fortes (dismenorreia).
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Sinais e sintomas
O que aparece no corpo e com que frequência cada sintoma acontece
Características mais comuns
Os sintomas variam de pessoa para pessoa. Abaixo estão as 1 características clínicas mais associadas, ordenadas por frequência.
Linha do tempo da pesquisa
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Genética e causas
O que está alterado no DNA e como passa nas famílias
Nenhum gene associado encontrado
Os dados genéticos desta condição ainda estão sendo catalogados.
Diagnóstico
Os sinais que médicos procuram e os exames que confirmam
Tratamento e manejo
Remédios, cuidados de apoio e o que precisa acompanhar
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Hospitais de referência no Brasil e o protocolo oficial do SUS (PCDT)
🇧🇷 Atendimento SUS — Septo vaginal transverso
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Publicações mais relevantes
Difficult Management of a Rare Case of Distal Vaginal Atresia in an Adolescent.
A transverse vaginal septum is a rare congenital anomaly that can present with primary amenorrhea and cyclic pelvic pain due to obstructive Müllerian malformation. We report the case of a 16-year-old adolescent who presented with primary amenorrhea and eight months of progressive cyclic lower abdominal pain. Physical examination revealed normal secondary sexual characteristics. Hormonal evaluation confirmed normal hypothalamic-pituitary-ovarian axis function. Pelvic MRI demonstrated hematometra and hematocolpos with a thin, regular vaginal septum and an associated distal vaginal agenesis component. Initial surgical correction was performed via vaginal approach, involving circumferential incision of the obstructive septum, controlled drainage of retained menstrual blood, complete excision of septal tissue, and end-to-end mucosal anastomosis. Despite initial resolution of symptoms and establishment of normal menstrual flow, the patient experienced recurrent obstruction at two months postoperatively, requiring vaginal dilation. At four months, she developed pelvic sepsis from infected hematocolpos, necessitating surgical revision with fibrotic tissue excision and attempted vaginal mold placement, which was poorly tolerated and removed after four days. This case highlights the challenging nature of complete transverse vaginal septum management, particularly when associated with distal vaginal agenesis. Despite appropriate initial surgical correction, a significant risk of stenosis, recurrent obstruction, and infectious complications exists, necessitating close postoperative surveillance and readiness for multiple interventions to achieve satisfactory long-term outcomes.
Reproductive outcomes after surgical correction of congenital obstructive genital tract anomalies: A systematic review and quantitative pooled analysis of published data.
Congenital obstructive genital tract anomalies are rare but clinically significant causes of menstrual outflow obstruction, endometriosis, and subfertility. Surgical correction aims to restore reproductive potential, yet evidence to guide counselling on fertility and pregnancy outcomes remains fragmented. To synthesise and pool published data on fertility, obstetric, and neonatal outcomes following surgical correction of congenital obstructive anomalies, comparing outcomes across anomaly types to inform individualised counselling. A systematic review was conducted. PubMed, Emcare, CINAHL, and Scopus were searched from inception to May 2025. Studies reporting reproductive outcomes after surgical correction of imperforate hymen, transverse vaginal septum, OHVIRA-spectrum, functional non-communicating uterine horns, or cervicovaginal atresia were included. Data were extracted independently and pooled by anomaly type. Study quality was assessed using Joanna Briggs Institute tools. Ninety-six studies (41 case reports, 41 case series, and 14 retrospective cohorts) were contributed 634 fertility-related events. Infertility rates were low following imperforate hymen (8.0%) and OHVIRA-spectrum anomalies (18.2%), intermediate in functional rudimentary horns (21.2%), and high following transverse vaginal septum (52.6%) and cervicovaginal atresia (55.4%). Among achieved pregnancies, livebirth rates exceeded 80%. Preterm birth occurred in 23.7% of pregnancies and did not differ significantly by anomaly type. Caesarean delivery was frequent (55.9%), particularly after cervicovaginal reconstruction (97.6%). Birthweight was lower following cervicovaginal atresia repair, with higher rates of small-for-gestational-age infants. Gestational hypertensive disorders were associated with co-existing renal agenesis. Reproductive outcomes after surgical correction are generally favourable but vary substantially by anomaly type. These findings support individualised counselling and targeted antenatal surveillance.
Recurrent Vulvovaginitis as an Unusual Presentation of Diagnosed Obstructed Hemivagina and Ipsilateral Renal Anomalies (OHVIRA) Syndrome in an Adolescent: A Case Report and Review of the Literature.
Background: Vulvovaginitis is a common condition in pediatric and adolescent female patients and is most frequently caused by infection. Although non-infectious etiologies are less common, they should be considered, particularly in cases that are refractory to standard treatment. Case: We report a rare case of a 16-year-old adolescent who was ultimately diagnosed with obstructed hemivagina and ipsilateral renal anomalies (OHVIRA) syndrome after experiencing recurrent vulvovaginitis for more than one year. Despite repeated antimicrobial treatments, her symptoms persisted. Further imaging studies revealed uterine didelphys with an obstructed hemivagina and ipsilateral renal agenesis. Surgical resection of the vaginal septum resulted in complete resolution of symptoms. Conclusions: Müllerian anomalies, such as OHVIRA syndrome, should be considered in the differential diagnosis for adolescents with recurrent vulvovaginitis refractory to conventional therapy. Delayed diagnosis may result in complications that significantly impair both quality of life and future reproductive potential.
When the path is blocked: A case of a transverse vaginal septum diagnosed in labor.
Transverse vaginal septa are rare, with incidence estimated to be between 1 in 30 000 to 1 in 84 000 people. Despite much literature in the gynecologic setting, there is little guidance about how to manage them when diagnosed in labor. A 23-year-old G1P000 patient presented to Labor and Delivery at 40 weeks 0 days with contractions and vaginal bleeding. A sterile bimanual exam found a blind vaginal ending, with no identifiable cervix. A point of care transvaginal ultrasound showed a transverse septum that measured 0.39 cm in thickness, with a normal cervix behind the septum. The patient was offered an exam under anesthesia with possible septum resection or primary cesarean delivery. She elected for an exam under anesthesia, which revealed a small area of dimpling on the septum. This was bluntly dissected along the scar of the previous resection, without hemorrhage or other complications. Subsequently, the cervix was identified, and the exam was 5 cm dilated, 80% effaced. The patient progressed to an uncomplicated vaginal delivery with no hemorrhage noted in the antepartum or postpartum period. Though there is no consensus or official recommendation for how to manage transverse vaginal septa during labor, there is a concern that a transverse vaginal septum during labor can lead to bleeding or obstructed labor, which can potentially result in uterine rupture. Our patient was diagnosed via transvaginal ultrasound, allowing for blunt dissection and ultimately an uncomplicated vaginal delivery; and this option should be considered for such patients identified in the intrapartum period.
Transverse vaginal septum with recurrent stricture formation in adolescence: a clinical challenge.
Transverse vaginal septum (TrVS) is a rare congenital anomaly of the Müllerian duct system that leads to obstructed menstrual flow. We present a case of a teenage girl with primary amenorrhoea, cyclic pelvic pain and a high transverse vaginal septum associated with haematocolpos and a septate uterus. Initial resection under laparoscopic guidance provided temporary relief, but postoperative complications such as vaginal stricture and adhesions developed due to non-compliance with dilation therapy. Secondary surgery involved stricture release and placement of a collagen-elastin scaffold (Matriderm) to prevent re-adhesion. At the 6 week follow-up, vaginal patency was maintained with restored menstruation. This case emphasises the need for structured follow-up and emerging reconstructive strategies for optimal outcomes. In 2021, the American Society of Reproductive Medicine (ASRM) Müllerian Anomalies Classification created 9 classifications: : Cervical agenesis. Müllerian agenesis. Unicornuate uterus. Bicornuate uterus. Septate uterus. Uterus didelphys. Longitucinal vaginal septum. Transverse vaginal septum. Complex anomalies . The most common subtype of Müllerian anomalies is the unification defect known as a bicornuate uterus (55.1%-73.5%). A bicornuate uterus arises from incomplete fusion of the paired Müllerian ducts during embryogenesis, typically between the sixth and tenth weeks of gestation. This anomaly results in a uterus with 2 distinct endometrial cavities and a single cervix, although variations exist (see Image. Uterus Embryology). Clinically, a bicornuate uterus is associated with an increased risk of infertility, recurrent pregnancy loss, preterm labor, malpresentation, and adverse obstetric outcomes. Accurate diagnosis, often requiring advanced imaging modalities such as 3D transvaginal ultrasound or magnetic resonance imaging (MRI), is essential to differentiate it from other uterine anomalies like a septate uterus, which has markedly different management implications. The risk of severe maternal morbidity for a bicornuate uterus is 3.0%.
Publicações recentes
Integration of 3D-printed simulation models into a PAG fellowship curriculum: impact on trainee confidence and curriculum acceptability.
Difficult Management of a Rare Case of Distal Vaginal Atresia in an Adolescent.
Reproductive outcomes after surgical correction of congenital obstructive genital tract anomalies: A systematic review and quantitative pooled analysis of published data.
Recurrent Vulvovaginitis as an Unusual Presentation of Diagnosed Obstructed Hemivagina and Ipsilateral Renal Anomalies (OHVIRA) Syndrome in an Adolescent: A Case Report and Review of the Literature.
When the path is blocked: A case of a transverse vaginal septum diagnosed in labor.
📚 EuropePMC118 artigos no totalmostrando 100
Difficult Management of a Rare Case of Distal Vaginal Atresia in an Adolescent.
CureusReproductive outcomes after surgical correction of congenital obstructive genital tract anomalies: A systematic review and quantitative pooled analysis of published data.
European journal of obstetrics, gynecology, and reproductive biologyRecurrent Vulvovaginitis as an Unusual Presentation of Diagnosed Obstructed Hemivagina and Ipsilateral Renal Anomalies (OHVIRA) Syndrome in an Adolescent: A Case Report and Review of the Literature.
Journal of clinical medicineWhen the path is blocked: A case of a transverse vaginal septum diagnosed in labor.
International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and ObstetricsTransverse vaginal septum with recurrent stricture formation in adolescence: a clinical challenge.
BMJ case reportsComplete transverse vaginal septum complicated by pyocolpos, primary vesicoureteral reflux and ectopic ureter with renal loss: a case report.
Urology case reportsMayer-Rokitansky-Kuster-Hauser syndrome.
Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e ObstetriciaFirst trimester suction aspiration without septum resection for transverse vaginal septum: A case report.
ContraceptionInverted Y-flap neovaginoplasty procedure combined with intracervical catheterization mold amnion graft in distal agenesis of vagina with transverse median vaginal septal: A case report.
International journal of surgery case reportsUterovaginal Anomalies in Pediatric Patients.
Journal of Indian Association of Pediatric SurgeonsImaging and Diagnostic Challenges in an 11-Year-Old Girl with Vaginal Agenesis: A Case Report.
The American journal of case reportsCongenital Uterine Anomaly with Concurrent Longitudinal and Transverse Vaginal Septa: Presentation of Two Cases.
Journal of pediatric and adolescent gynecologyFrequency, clinical presentation and management of primary amenorrhea in a tertiary care setting.
Pakistan journal of medical sciencesCongenital Abnormalities Causing Hematocolpos: A Pictorial Essay.
Journal of the Belgian Society of RadiologyUterine didelphys with transverse vaginal septum in a 16-year-old female: the third case report in the medical literature.
Journal of surgical case reportsA Full-Term Pregnancy in a Patient With Uterus Didelphys.
CureusComparison between 3D-Enhanced Conventional Pelvic Ultrasound and Magnetic Resonance Imaging in the Evaluation of Obstructive Müllerian Anomalies and Its Concordance with Surgical Diagnosis.
Journal of pediatric and adolescent gynecologyCaudal regression syndrome associated with obstructive genital tract anomaly.
BMJ case reportsMultimodality imaging of acute gynecological emergencies-a pictorial essay.
Abdominal radiology (New York)Successful correction of the transverse vaginal septum with a pinhole vaginal foramen using Y-V plasty: A case report.
Case reports in women's healthA Rare Case of Hematometrocolpos due to Transverse Vaginal Septum along with Distal Vaginal Atresia in an Adolescent Girl.
Journal of the West African College of SurgeonsHigh imperforate transverse vaginal septum with vaginal cicatrisation: a surgical tribulation.
BMJ case reportsMultimodality imaging of diseases of the vagina.
The British journal of radiologyLaparoscopic Uterine Preservation and Vaginal Reconstruction in a 13-Year-Old Girl with Uterus Didelphys, Bilateral Vesicovaginal Fistulas, and Transverse Vaginal Septum.
Journal of pediatric and adolescent gynecologyAn unusual case report of transverse vaginal septum presenting as primary amenorrhea.
International journal of surgery case reportsSuccessful Use of Acellular Small Intestinal Submucosa Graft in Vaginal Reconstruction.
Journal of pediatric surgerySurgical management of a transverse vaginal septum: About a rare case.
International journal of surgery case reportsMinimally Invasive Surgery for Transverse Vaginal Septum in an Adolescent Girl.
Journal of minimally invasive gynecologyObstructed hemivagina and ipsilateral renal agenesis: magnetic resonance imaging findings in young Nepali females - a report of four cases.
Annals of medicine and surgery (2012)Retention of a Foreign Body in the Vagina of an Adult for 13 Years: A Case Report.
CureusPancake kidney with a single ureter, hydrometrocolpos, and imperforate anus: a set of uncommon malformations in a female adolescent.
Archivos argentinos de pediatriaRare Transverse Vaginal Septum in an Adolescent Girl.
CureusConception following successful repair of two previous failed attempts at repair of partial transverse vaginal septum diagnosed after marital union: A case report.
SAGE open medical case reportsCase report: Hydrometrocolpos conditioning recurrent urinary tract infections.
Frontiers in surgeryForty-two normomenstruating adolescents with Müllerian obstructive anomalies: Presentation, pitfalls in the dagnosis and surgical management.
Acta obstetricia et gynecologica ScandinavicaFamilial occurrence of concomitant imperforate hymen and transverse vaginal septum: a case report.
The Pan African medical journalCase series: Interdigitating "Y" flap for transverse vaginal septum management.
International journal of surgery case reportsMayer-Rokitansky-Kuster-Hauser Syndrome: A rare case report from Nepal.
Annals of medicine and surgery (2012)Management of an isolated complete imperforate transverse vaginal septum: A case report.
International journal of surgery case reportsYoung adolescent with trisomy 13.
BMJ case reportsSurgical disorders in pediatric and adolescent gynecology: Vaginal and uterine anomalies.
International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and ObstetricsNeonatal hydrocolpos presenting as a rapidly progressive abdominal mass with inferior caval vein syndrome.
BMJ case reportsRobotic management of congenital urethra-vaginal fistula with transverse vaginal septum.
International braz j urol : official journal of the Brazilian Society of UrologyAsymptomatic microperforated transverse vaginal septum.
Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and GynaecologyTransverse Vaginal Septum Resection: Technique, Timing, and the Utility of Dilation. A Scoping Review of the Literature.
Journal of pediatric and adolescent gynecologyHematometrocolpos following Low Transverse Cesarean Delivery Complicated by Uterine Dehiscence.
Case reports in obstetrics and gynecologyTransverse vaginal septum managed by simple flap surgery technique: A case report.
International journal of surgery case reportsMimics of malignancy caused by concurrent imperforate hymen and transverse vaginal septum: an instructive case and review of the literature.
The Journal of international medical researchCongenital anomalies causing hemato/hydrocolpos: imaging findings, treatments, and outcomes.
Japanese journal of radiologyManagement of a transverse vaginal septum complicated with hematocolpos in an adolescent girl: Case report.
International journal of surgery case reportsUterine Didelphys with Transverse Vaginal Septum - A Complex Rare Müllerian Anomaly.
Acta medica LituanicaRecurrent obstructive uropathy secondary to pyometrocolpos in an 8-month-old infant: a case report.
Journal of medical case reportsOutpatient abortion in a patient with a previously undiagnosed transverse vaginal septum: A case report.
ContraceptionThe first major complication due to laser treatment for stress urinary incontinence: a short report.
Climacteric : the journal of the International Menopause SocietyTransverse vaginal septum presenting as secondary amenorrhoea: a rare clinical presentation.
BMJ case reportsLaparoscopic Colpo-Pneumo Occluder as a Vaginal Mold for Vaginal Reconstruction.
Journal of pediatric and adolescent gynecologyManagement of Mullerian Development Anomalies: 9 Years' Experience of a Tertiary Care Center.
Gynecology and minimally invasive therapyTransverse Vaginal Septum with a Hemiuterus: A Laparoscopic-Guided Abdominoperineal Approach.
Journal of pediatric and adolescent gynecologyPrimary amenorrhea in females attending gynaecological outpatient of a tertiary care hospital at Peshawar.
JPMA. The Journal of the Pakistan Medical AssociationPerforated Transverse Vaginal Septum in a Virgin Patient: A Hymen-sparing Hysteroscopic-ultrasound-guided Approach.
Journal of minimally invasive gynecologyDiagnosis and treatment of müllerian malformations.
Taiwanese journal of obstetrics & gynecologyCongenital vaginal obstruction in a newborn.
Sudanese journal of paediatricsApplication of Saline Infusion Sonocolpography in Diagnosis and Treatment of Perforated Transverse Vaginal Septum.
Case reports in obstetrics and gynecologyAsymptomatic microperforated transverse vaginal septum presenting with primary infertility: a rare form of mullerian anomaly.
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Fertility and sterilitySolid Pseudopapillary Neoplasm of the Pancreas in a Pediatric Patient with Associated Urogenital Anomalies.
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Journal of human reproductive sciencesUrinary presentations of a posttraumatic vaginal septum in a 14-year-old girl.
Turkish journal of urologyManagement of Transverse Vaginal Septum by Vaginoscopic Resection: Hymen Conservative Technique.
Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e ObstetriciaHaematometrocolpos due to transverse vaginal septum with distal atretic vagina.
BMJ case reportsIntralesional Steroid Injections for Recurrent Vaginal Strictures.
Journal of pediatric and adolescent gynecologyA CASE REPORT OF PREMENARCHIAL TRANSVERSE VAGINAL SEPTUM AT THE UNIVERSITY COLLEGE HOSPITAL, IBADAN.
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Taiwanese journal of obstetrics & gynecologyDouble mucosal flap for the reconstruction of transverse vaginal septum - A novel surgical approach using the vaginal septal tissue.
Urology case reportsTransverse Vaginal Septum: Report of Two Patients with MRI Findings.
Journal of the College of Physicians and Surgeons--Pakistan : JCPSPTransverse vaginal septum identified in a patient requesting second trimester abortion: a case report.
ContraceptionClinical and radiological findings for early diagnosis of Herlyn-Werner-Wunderlich syndrome in pediatric age: experience of a single center.
Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology[Transverse vaginal septum diagnosed in sisters. Cases report].
Archivos argentinos de pediatriaGynecologic Surgery: Preoperative Assessment With Ultrasound.
Clinical obstetrics and gynecologyThe Use of Vaginal Mold Following Resection of Transverse Vaginal Septum as Treatment Approach to Patient With Multiple Failed Attempts to Resolve Recurrent Hematocolpos.
Journal of minimally invasive gynecologyThe interdigitating Y-plasty procedure for the correction of transverse vaginal septa.
BJOG : an international journal of obstetrics and gynaecologyLow complete transverse vaginal septum, vesico-ureteric reflux and low anorectal malformation: Case report and review of literature.
International journal of pediatrics & adolescent medicineCongenital urethrovaginal fistula with transverse vaginal septum.
The journal of obstetrics and gynaecology researchRare combination of anomalies and its management with conservative and effective approach.
Journal of human reproductive sciencesTransverse Vaginal Septum With Secondary Infertility: A Rare Case.
Journal of minimally invasive gynecologyTreatment of Virgin OHVIRA Syndrome with Haematometrocolpos by Complete Incision of Vaginal Septum without Hymenotomy.
Journal of clinical and diagnostic research : JCDRRare Müllerian Anomaly: Complete Septate Uterus with Simultaneous Longitudinal and Transverse Vaginal Septa.
Journal of pediatric and adolescent gynecologyDouble Cross Plasty for Management of Transverse Vaginal Septum: A 20-Year Retrospective Review of Our Experience.
Journal of obstetrics and gynaecology of IndiaManagement of Recurrent Stricture Formation after Transverse Vaginal Septum Excision.
Case reports in obstetrics and gynecologyBowel vaginoplasty in children and young women: an institutional experience with 55 patients.
International urogynecology journalA rare case of primary amenorrhea with two etiologies, hypothalamic amenorrhea, transverse vaginal septum, and no hematocolpos.
Case reports in obstetrics and gynecologyCase of early postoperative adhesion in a patient with molimina due to transverse vaginal septum concomitant with imperforate hymen.
The journal of obstetrics and gynaecology researchSuccessful pregnancy outcome in an untreated case of concomitant transverse complete vaginal septum with unicornuate uterus.
Journal of human reproductive sciencesAssociações
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Referências e fontes
Bases de dados externas citadas neste artigo
Publicações científicas
Artigos indexados no PubMed ligados a esta doença no grafo RarasNet — título, periódico e PMID direto da fonte, sem intermediação de IA.
- Difficult Management of a Rare Case of Distal Vaginal Atresia in an Adolescent.
- Reproductive outcomes after surgical correction of congenital obstructive genital tract anomalies: A systematic review and quantitative pooled analysis of published data.European journal of obstetrics, gynecology, and reproductive biology· 2026· PMID 41713152mais citado
- Recurrent Vulvovaginitis as an Unusual Presentation of Diagnosed Obstructed Hemivagina and Ipsilateral Renal Anomalies (OHVIRA) Syndrome in an Adolescent: A Case Report and Review of the Literature.
- When the path is blocked: A case of a transverse vaginal septum diagnosed in labor.International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics· 2026· PMID 41236838mais citado
- Transverse vaginal septum with recurrent stricture formation in adolescence: a clinical challenge.
- Integration of 3D-printed simulation models into a PAG fellowship curriculum: impact on trainee confidence and curriculum acceptability.
Bases de dados e fontes oficiais
Identificadores e referências canônicas usadas para montar este verbete.
- ORPHA:180160(Orphanet)
- MONDO:0015850(MONDO)
- GARD:20191(GARD (NIH))
- Busca completa no PubMed(PubMed)
- Q55785772(Wikidata)
Dados compilados pelo RarasNet a partir de fontes abertas (Orphanet, OMIM, MONDO, PubMed/EuropePMC, ClinicalTrials.gov, DATASUS, PCDT/MS). Este conteúdo é informativo e não substitui avaliação médica.
Conteúdo mantido por Agente Raras · Médicos e pesquisadores podem colaborar
