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Littérature scientifique sur le sujet « EXSTROPHY »

Auteur : Grafiati
Publié le 1 avril 2023

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Articles de revues sur le sujet "EXSTROPHY"

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Thapa, Bijay. « Duplicate Bladder Exstrophy With Fistula : A Rare Variant of Exstrophy-Epispadias Complex ». Journal of Nepal Paediatric Society 41, no 2 (3 novembre 2021) : 282–85. http://dx.doi.org/10.3126/jnps.v41i2.30752.

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Variants of exstrophy are rare anomalies seen in the spectrum of bladder exstrophy-epispadias complex. A seven day old male neonate was admitted in our department with a rare variant of duplicate bladder communicating with exstrophy bladder with fistula. Patient presented with patch of exstrophic bladder just below the low set umbilicus with a normal sized phallus and normally positioned urethral meatus. The baby was managed successfully with surgery and is under regular follow up.
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Ben-Chaim, Jacob, Steven G. Docimo, Robert D. Jeffs et John P. Gearhart. « Bladder Exstrophy from Childhood into Adult Life ». Journal of the Royal Society of Medicine 89, no 1 (janvier 1996) : 39P—46P. http://dx.doi.org/10.1177/014107689608900112.

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Exstrophy of the bladder is rare and the incidence of bladder exstrophy is calculated to be from 1 per 30 000 to 50 000 live births with male to female ratio ranging from 1.5-5 to 1 1-4 It was found that persistence or overgrowth of the cloacal membrane on the lower anterior abdominal area, prevents normal mesenchymal ingrowth. This causes divergence of the lower abdominal muscular structures and forces the genital ridges to fuse caudal to the cloacal membrane. The stage of ingrowth of the urorectal septum at the time of rupture determines whether one will produce an exstrophic urinary tract alone (classic bladder exstrophy or epispadias) or cloacal exstrophy with the hindgut interposed between the hemibladders5,6.
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Ahmed et Abu Daia. « Exstrophic abdominal wall defect without bladder exstrophy (pseudo-exstrophy) ». BJU International 81, no 5 (mai 1998) : 762–63. http://dx.doi.org/10.1046/j.1464-410x.1998.00584.x.

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van der Putte, S. C. J., W. G. M. Spliet et P. G. J. Nikkels. « Common (“Classical”) and Covered Cloacal Exstrophy : A Histopathological Study and a Reconstruction of the Pathogenesis ». Pediatric and Developmental Pathology 11, no 6 (novembre 2008) : 430–42. http://dx.doi.org/10.2350/07-06-0292.1.

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Current opinion about structure and pathogenesis of cloacal exstrophy was challenged by histopathological findings and new insights into the normal development. Autopsy specimens of common ( n = 3) and covered cloacal exstrophy ( n = 4) with single intraexstrophic and -perineal phallic structures and perineo-exstrophic canals have been analyzed histopathologically. The findings were correlated to normal development to reconstruct the pathogenesis. By identifying a specific cloaca-derived urethra field as distinct from allantois-derived bladder fields, the exstrophic area is found to reflect the original hindgut configuration in embryos of approximately 26–29 postovulatory days gestational age (2–4 mm). Correlation to normal development suggests malfunctioning of the primitive streak/caudal eminence as a primary fault that leads to a defective cloacal region in the hindgut disturbing cloacal-intestinal-allantoic dissociation and also causes lengthening of the intestinal region into a blind-ending colon, teratoma-like lesions, and vertebral and muscular anomalies. The current idea that membranes in “covered cloacal exstrophy” represent persisting cloacal membranes is dismissed by finding an amnion-like structure, which suggests dysfunction of an umbilical ring placode as a simultaneous 2nd fault. This malfunctioning may cause omphalocele by defective demarcation of the umbilical cord and may replace midline stroma of the infraumbilical abdominal wall by extraembryonic tissue that stretches into a weak temporary membrane, may leave a perineo-extrophic canal, and may allow the formation of a single perineal or intraexstrophic phallus. Malfunctioning without replacement may result in a purely epithelial “allantoic” membrane, which by disintegrating in combination with the cloacal membrane will expose common cloacal exstrophy.
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Ganarin, Alba, Michele Corroppolo, Giosuè Mazzero, Clara Revetria, Fabio Beretta et Enrico Ciardini. « Exstrophy-Epispadias Complex Variants : A Hybrid Case ». Pediatric Reports 13, no 2 (7 avril 2021) : 177–80. http://dx.doi.org/10.3390/pediatric13020024.

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The term exstrophy-epispadias complex refers to a group of midline defects ranging from epispadias to cloacal exstrophy. Bladder exstrophy is the most frequent malformation of this spectrum and it can present as a classical or a variant form. We report a case of a hybrid bladder exstrophy variant having some characteristics of both a duplicate bladder exstrophy and a superior vesical fistula.
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Inouye, Brian M., Ali Tourchi, Heather N. Di Carlo, Ezekiel E. Young et John P. Gearhart. « Modern Management of the Exstrophy-Epispadias Complex ». Surgery Research and Practice 2014 (2014) : 1–9. http://dx.doi.org/10.1155/2014/587064.

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The exstrophy-epispadias complex is a rare spectrum of malformations affecting the genitourinary system, anterior abdominal wall, and pelvis. Historically, surgical outcomes were poor in patients with classic bladder exstrophy and cloacal exstrophy, the two more severe presentations. However, modern techniques to repair epispadias, classic bladder exstrophy, and cloacal exstrophy have increased the success of achieving urinary continence, satisfactory cosmesis, and quality of life. Unfortunately, these procedures are not without their own complications. This review provides readers with an overview of the management of the exstrophy-epispadias complex and potential surgical complications.
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Thakkar, Nirali Chirag, Prince Raj et Yogesh Kumar Sarin. « Antero-posterior Duplicate Exstrophy with a Wet Bladder Plate : A Diagnostic Dilemma ». Journal of Neonatal Surgery 5, no 3 (1 juillet 2016) : 37. http://dx.doi.org/10.21699/jns.v5i3.369.

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Variants of exstrophy are rare anomalies seen in the spectrum of bladder exstrophy-epispadias complex. We present a rare case of duplicate exstrophy with a wet bladder plate. This is a deviation from the classical description of antero-posterior duplicate exstrophy that is associated with a dry bladder plate.
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Patil, Prashant Sadashiv, Paras Kothari, Abhaya Gupta, Rahul Gupta, Geeta Kekre, Vishesh Dikshit et Ravi Kamble. « Cloacal Exstrophy with Mature Teratoma : A Rare Association in a Neonate ». Journal of Neonatal Surgery 5, no 2 (13 mars 2016) : 17. http://dx.doi.org/10.47338/jns.v5.284.

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Cloacal exstrophy is a very rare and complex malformation. We report a neonate of cloacal exstrophy with mature teratoma presenting as a component of exstrophy. To our knowledge this has not been reported in the literature.
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Aboushaer, Mohamed B., et Noura M. Almutairi. « Cloacal exstrophy misdiagnosed as bladder exstrophy ». Journal of Pediatric Surgery Case Reports 56 (mai 2020) : 101425. http://dx.doi.org/10.1016/j.epsc.2020.101425.

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Vilanova-Sánchez, Alejandra, Christina Ching, Alessandra Gasior, Karen Diefenbach, Richard Wood et Marc Levitt. « Image of the Month : Clinical Features in a Newborn with Covered Cloacal Exstrophy ». European Journal of Pediatric Surgery Reports 05, no 01 (janvier 2017) : e57-e59. http://dx.doi.org/10.1055/s-0037-1606389.

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AbstractCloacal exstrophy is the most severe type of anorectal malformations that belongs to the bladder–exstrophy–epispadias complex of genitourinary malformations. Interestingly, its variant, the covered cloacal exstrophy, is often missed. The clinical findings of this variant may include an imperforate anus, low lying umbilicus, thick pubic bone, and pubic diastasis but with an intact abdominal wall. We present an interesting case of covered cloacal exstrophy with a side-by-side duplicated bladder and discuss important considerations for the time of colostomy creation in the newborn period.
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Thèses sur le sujet "EXSTROPHY"

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Clementson, Kockum Christina. « Bladder exstrophy clinical and experimental aspects / ». Lund : University Hospital, Dept. of Paediatric Surgery, 1998. http://catalog.hathitrust.org/api/volumes/oclc/68945118.html.

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Anderson, Deborah. « Making sense of intimacy and sexual health for people with exstrophy-epispadias complex conditions ». Thesis, Lancaster University, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.586929.

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This doctoral thesis explores how people with exstrophy-epispadias complex (EEC) conditions (including bladder exstrophy) experience intimate relationships. It includes a literature review, a research paper, a critical review, and an ethics section. The literature review takes a critical look at the current conceptualisation of sexuality for people with EEC through critique of the current EEC literature. As such, it argues that this current conceptualisation lacks sufficient consideration for psychological and social factors. Relevant findings from within related health psychology research are used to demonstrate the need for these factors to be considered. Furthermore, it is suggested that a new conceptualisation of sexual health should be adopted in order to incorporate these factors into both research and clinical practice. Finally, the implications of this potential change are discussed with consideration for how potential barriers may be overcome. The research paper leads on from this argument by adopting a qualitative approach to exploring an important psychological element of sexual health. Previous findings have suggested that people with bladder exstrophy and other EEC conditions have difficulties establishing and maintaining intimate relationships with friends or romantic partners. An interpretative phenomenological analysis was conducted with data from six participants with bladder exstrophy. Findings were described within three themes; 'exploring intimacy from a position of safety', 'the relationship between intimacy with the self and intimacy with others', and 'the magical value of intimacy: sharing the full story of bladder exstrophy'. Findings are discussed in relation to previous research and theory regarding concealment, body shame, and the development of identity, and clinical implications are presented. Finally, the critical review reflects on some of the key issues of relevance to carrying out this research. These include methodological issues related to analytical approach, homogeneity and data collection, and further reflection on the process of analysis.
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Dix-Peek, Stewart. « Pelvic osteotomies for exstrophy : a review of techniques and outcomes at Red Cross Children's Hospital ». Master's thesis, University of Cape Town, 2007. http://hdl.handle.net/11427/2838.

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Kertai, Michael [Verfasser], et Wolfgang H. [Akademischer Betreuer] Rösch. « Morphological and Functional Hip Long-Term Results after Exstrophy Repair / Michael Kertai ; Betreuer : Wolfgang H. Rösch ». Regensburg : Universitätsbibliothek Regensburg, 2016. http://d-nb.info/112380270X/34.

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Berrettini, Alfredo. « Long term outcomes in terms of sexual function and relational aspects in primary cases born with Bladder Exstrophy ». Doctoral thesis, Università degli studi di Padova, 2013. http://hdl.handle.net/11577/3422993.

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Introduction and purpose Bladder exstrophy (BE) is a rare malformation that involves not only the bladder, urethra and genital organs but also all of the pelvic floor and bones. Its prevalence is about 1/25.000-40.000 born in Italy and about 15 new cases are estimated each year. The disease affects males and females with a ratio of 2:1. The etiology is unknown. The effect of this malformation, affecting the urogenital complex, can be reflected on urinary continence and sexual life. These aspects can influence strongly the social life of patients. We evaluated both psychosexual and psychosocial aspects and sexual dysfunctional in adult with BE using a validated instrument. Materials and methods We conducted a survey using SESAMO (Sexuality Evaluation Schedule Assessment Monitoring). We evaluated a group of patients (cases) and a group of controls. All are invited to complete the male or female, single or partnership version of the instrument. The questionnaires are loaded into the program SESAME-Win and processed by the software SESAME-R. Both cases and the controls are analyzed in general and by sex and by emotional situation (single or partnership). We investigated the Areas found to be significant in the group of cases and not in the corresponding group of controls; in these Areas we analyzed individually every Items, highlighting the percentage of significant responses. We also assessed the state of continence about patients. Results This questionnaire is being distributed to 45 patients with BE, including 30 men (M) and 15 women (W) and 40 controls, 20 M and 20 W. 26 cases (17 M and 9 W), with a response rate of 57.7%, and 35 controls (18 M and 17 W) with a response rate of 87.5%, were finally included in analysis. With regard to the cases 16 (11 M and 5 W), completed the questionnaire as situation of “partnership” and 10 (6 M and 4 W) as "single". In group of controls 26 (14 M and 12 W) completed the questionnaire as situation of "partnership" and 9 (4 M and 5 W) as "single". Median age was 28 years in the Cases group and 30.5 in Controls. Environmental psychology and Lived Body Areas were significant in all groups of Cases (except in Females Total about Lived Body) and never in groups of controls. Desire Area is significant only in females Cases. Pleasure Areas are significant only in the groups of Controls and never in Cases. Remote Masturbation is significant, both in the group of Cases that Controls Females. Previous Experiential and the Sexual and Medical History are significant in all groups (except in the group of females controls about this last Area). Patients had a continence rate of 80, 7%. Conclusions Patients with bladder exstrophy have a tendency toward obsessive-compulsive disorder towards sexuality. They are dissatisfied about their free time, but they reached a satisfactory social position. They have a critical relationship with their parents and especially with mother, certainly more present in the clinical pathway. Especially with female patients, there is a lack of communication about sexuality. They present a difficulty to express and share their experiences, particularly sexuality, which they define like frustration experience. The body perception was very critical, more critical in single cases than in partnership. The areas of the body affected by the malformation are hated by themselves. Sexual dysfunction affects a high percentage of both sexes and the women seem to have more difficulty in having a satisfying sexual relationship. Sexuality appear a pathological experience in both single and partnership group. Singles are not satisfied with their emotional situation and even the frequency of sexual intercourse. Patients who live in a partnership use frequently masturbation not for his own pleasure but as act that substitute a complete sexual intercourse.
Introduzione e scopo dello studio L’Estrofia Vescicale-Epispadia (EV) è una rara patologia congenita caratterizzata da uno sviluppo incompleto della vescica e dell’uretra. La sua prevalenza varia da 1/25.000 a 1/40.000 nati ed in Italia si stima un'incidenza di circa 15 nuovi casi ogni anno. La patologia colpisce maschi e femmine con un rapporto di 2:1. L’etiologia non è nota. La patologia, colpendo l’apparato uro-genitale si riflette su elementi di primaria importanza, vale a dire la continenza urinaria e la vita sessuale. Tali aspetti possono condizionare fortemente la vita di relazione dei soggetti affetti. Scopo dello studio è stato quello di identificare sia gli aspetti psicosessuali e psicosociali che gli aspetti disfunzionali sessuali in soggetti affetti da EV. Materiali e metodi Abbiamo eseguito un’indagine strutturata mediante il questionario SESAMO (Sexuality Evaluation Schedule Assessment Monitoring - Boccadoro, Perillo 1996). Sono stati individuati due gruppi d’indagine: un gruppo di pazienti (casi) e uno di soggetti non portatori della patologia (controlli). Tutti i soggetti sono stati invitati a rispondere alla versione maschile o femminile, single o di coppia del questionario. I questionari sono stati caricati nel programma SESAMO-Win ed elaborati dal software SESAMO-R. Sia i Casi che i controlli sono stati analizzati sia in generale che divisi per sesso e situazione affettiva single/coppia. Sono state indagate le Aree risultate significative nel gruppo dei Casi e non nel corrispettivo gruppo dei Controlli; di tali Aree sono stati analizzati singolarmente i vari Item che le componevano, evidenziando la percentuale di risposte significative. Abbiamo inoltre valutato lo stato di continenza dei pazienti. Risultati Il questionario è stato consegnato a 45 pazienti affetti da EV di cui 30 maschi (M) e 15 femmine (F) e 40 controlli, di cui 20 M e 20 F. Hanno aderito allo studio 26 casi (17 M e 9 F), con un tasso di risposta di 57,7%, e 35 controlli (18 M e 17 F) con un tasso di risposta di 87,5%. In particolare per quanto riguarda i casi, 16 (61,5%) di cui 11 M e 5 F, hanno compilato il questionario come situazione affettiva di “coppia” e 10 (38,5%) di cui 6 M e 4 F come “single”; riguardo i controlli 26 (74,5%) (14 M e 12 F) hanno compilato il questionario come situazione affettiva di “coppia” e 9 (25,5) (4 M e 5 F) come “single”. L’età mediana è stata di 28 anni nel gruppo dei casi e 30,5 nei controlli. Le Aree Relati psicoambientali e Vissuto corporeo sono risultate significative in tutti i gruppi dei Casi (eccetto nei Casi Femmine totali per quanto riguarda il vissuto corporeo) e mai nei gruppi dei Controlli. L’Area Desiderio è significativa solo nei Casi Femmine. Gli Ambiti del piacere sono significativi solo nei gruppi dei Controlli e mai nei Casi. La Masturbazione remota è significativa sia nel gruppo dei Casi che dei Controlli Femmine. L’Esperienziale pregresso e l’ Anamnesi Medica e Sessuale sono significative in tutti i gruppi (eccetto nel gruppo dei Controlli Femmine per quest’ultima Area). I pazienti hanno presentato un tasso di continenza dell’80,7%. Conclusioni I pazienti affetti da estrofia vescicale presentano una spiccata tendenza all’ossessività che si manifesta sia nelle pratiche quotidiane che nei confronti della sessualità. Sono insoddisfatti del loro tempo libero ma circa la metà di essi ha raggiunto una condizione sociale soddisfacente. Presentano un rapporto critico con i propri genitori e in particolar modo con la madre, figura sicuramente più presente nel percorso clinico; specialmente nelle pazienti di sesso femminile si riscontra una carente comunicazione intrafamiliare riguardo alla sessualità. E’ emersa inoltre una difficoltà ad esprimere e raccontare le loro esperienze, in particolare quelle sessuali che definiscono frustranti. L’attenzione rivolta al “se’ corporeo” è risultata molto critica, più nei casi in situazione di coppia che nei single; le zone interessate dalla malattia e di conseguenza coinvolte negli interventi chirurgici sono le più odiate da essi. Le disfunzioni sessuali colpiscono in alta percentuale entrambi i sessi e nel complesso le donne sembrano avere più difficoltà ad avere un rapporto sessuale soddisfacente. La sessualità è vissuta in maniera patologica sia nel gruppo dei pazienti “single” che “coppie”. I pazienti single non sono soddisfatti della loro situazione affettiva e neppure della frequenza dei rapporti sessuali. I pazienti che vivono una situazione di coppia sono spinti ad attuare con maggiore frequenza la masturbazione non per proprio piacere ma come atto sostitutivo al rapporto sessuale completo.
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Baker, Dawn. « Inside out : an exploratory study into the quality of life, psychological wellbeing, social competence and gender identity in children with cloacal exstrophy ». Thesis, University of East London, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.532467.

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Cordeiro, Tânia Gonçalves. « Exstrophy-epispadias complex : surgical management and outcome review ». Master's thesis, 2014. https://repositorio-aberto.up.pt/handle/10216/76075.

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Cordeiro, Tânia Gonçalves. « Exstrophy-epispadias complex : surgical management and outcome review ». Dissertação, 2014. https://repositorio-aberto.up.pt/handle/10216/76075.

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Livres sur le sujet "EXSTROPHY"

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Gearhart, John P., et Ranjiv Mathews, dir. The Exstrophy—Epispadias Complex. Boston, MA : Springer US, 1999. http://dx.doi.org/10.1007/978-1-4757-3056-2.

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Butler, Mary. Born to die ? Dublin : Marino Books, 1995.

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Bryant, Jason. Bladder Exstrophy. Sous la direction de Kirk Lalwani, Ira Todd Cohen, Ellen Y. Choi et Vidya T. Raman. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190685157.003.0040.

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Bladder exstrophy is a rare condition in which there is an error in fetal development leaving the bladder and pelvic structure malformed. The bladder, pelvic girdle, and external genitalia are often split, requiring repair. The goals of this repair are to improve quality of life in terms of urinary continence, aesthetics, pelvic stabilization, and sexual function. This repair often requires prolonged traction and external fixation to adequately fuse the pelvic girdle. To aid in the healing and tolerance of this, a prolonged epidural catheter is often used. The pharmokinetics and risk of infection are major considerations during the prolonged use of a caudal catheter.
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Transplantation of ureters into the rectum for exstrophy of the bladder, by the author's extraperitoneal method : Three additional cases. [Toronto ? : s.n., 1997.

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Transplantation of ureters into rectum by an extraperitoneal method for exstrophy of bladder, and a new operation for procidentia recti in the same patient. [S.l : s.n., 1997.

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Gearhart, John P., et Ranjiv Mathews. Exstrophy-Epispadias Complex : Research Concepts and Clinical Applications. Springer, 2010.

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Gearhart, John P., et Ranjiv Mathews. Exstrophy--Epispadias Complex : Research Concepts and Clinical Applications. Springer London, Limited, 2013.

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(Editor), John P. Gearhart, et Ranjiv Mathews (Editor), dir. The Exstrophy-Epispadias Complex : Research Concepts and Clinical Applications. Springer, 1999.

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Cuckow, Peter. Abnormalities of the bladder. Sous la direction de David F. M. Thomas. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199659579.003.0120.

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Anatomical and functional reconstruction of the bladder exstrophy/epispadias complex of anomalies presents paediatric urologists with one of their greatest challenges. Nevertheless, very considerable advances have been made during the last 30 years. Children with classic bladder exstrophy now have an excellent prospect of becoming fully continent—either by primary reconstruction or with a catheterizeable stoma. Achieving continence and normal voiding in children with primary epispadias can be difficult because of the dysplastic nature of their sphincteric and bladder neck tissues. Urachal anomalies may present symptomatically in childhood or incidentally during ultrasound examination of the lower urinary tract. Small bladder diverticula which are secondary to outflow obstruction or bladder dysfunction tend to resolve following treatment of the underlying cause, whereas surgical excision is usually required for larger, symptomatic diverticula.
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Mano, Roy, et Ofer Yossepowitch. Adenocarcinoma of the bladder. Sous la direction de James W. F. Catto. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199659579.003.0081.

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Adenocarcinoma of the bladder accounts for 0.5–2 of bladder tumours. Risk factors include bladder exstrophy, bladder augmentation, schistosomiasis, and endometriosis. Bladder adenocarcinoma is classified as primary, arising from the bladder or urachal remnant, and secondary (metastatic). Most patients present with haematuria and irritative voiding symptoms. On imaging, a typical lesion is commonly located at the bladder dome. Compared to urothelial carcinoma (UC), most adenocarcinomas are diagnosed at high grade and advanced stage. Surgical treatment of localized disease entails partial cystectomy for urachal tumours and radical cystectomy for non-urachal or large urachal adenocarcinoma. The optimal treatment for metastatic disease has yet to be defined. Overall survival rates are 20–70% at 5 years, similar to those for UC, when adjusted for stage and grade. Secondary adenocarcinomas commonly arise from a genitourinary or gastrointestinal origin. Differentiation from primary tumours may be complex. Treatment depends on the prognosis of the primary cancer.
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Chapitres de livres sur le sujet "EXSTROPHY"

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Peña, Alberto, et Andrea Bischoff. « Cloacal Exstrophy and Covered Cloacal Exstrophy ». Dans Surgical Treatment of Colorectal Problems in Children, 285–97. Cham : Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-14989-9_17.

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More, Bharat, et Imran Mushtaq. « Bladder Exstrophy, Epispadias, and Cloacal Exstrophy ». Dans Handbook of Pediatric Surgery, 313–19. London : Springer London, 2010. http://dx.doi.org/10.1007/978-1-84882-132-3_45.

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Novak, Thomas E., et Yegappan Lakshmanan. « Bladder Exstrophy ». Dans Pediatric Urology for the Primary Care Physician, 111–17. New York, NY : Springer New York, 2014. http://dx.doi.org/10.1007/978-1-60327-243-8_15.

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North, Amanda C., et John P. Gearhart. « Bladder Exstrophy ». Dans Pediatric Surgery, 629–34. Berlin, Heidelberg : Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-69560-8_64.

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Ziegler, Moritz M. « Cloacal Exstrophy ». Dans Pediatric Surgery, 635–42. Berlin, Heidelberg : Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-69560-8_65.

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Arap, Sami, et Amilcar M. Giron. « Bladder Exstrophy ». Dans The Exstrophy—Epispadias Complex, 111–15. Boston, MA : Springer US, 1999. http://dx.doi.org/10.1007/978-1-4757-3056-2_18.

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Hendren, W. Hardy, Robert E. Gross et Dennis P. Lund. « Cloacal Exstrophy ». Dans The Exstrophy—Epispadias Complex, 221–36. Boston, MA : Springer US, 1999. http://dx.doi.org/10.1007/978-1-4757-3056-2_33.

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Gatti, John M., et David Juang. « Cloacal Exstrophy ». Dans Fundamentals of Pediatric Surgery, 745–50. Cham : Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-27443-0_93.

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Carr, Michael C. « Cloacal Exstrophy ». Dans Fundamentals of Pediatric Surgery, 685–91. New York, NY : Springer New York, 2010. http://dx.doi.org/10.1007/978-1-4419-6643-8_88.

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Al-Salem, Ahmed H. « Cloacal Exstrophy ». Dans An Illustrated Guide to Pediatric Urology, 415–21. Cham : Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-44182-5_18.

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Actes de conférences sur le sujet "EXSTROPHY"

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Gurskaya, Alexandra, Olga Mokrushina, Oleg Nakovkin, Maria Sulavko, Dinara Akhmedova, Aram Tarzyan, Natalya Zhurkova, Kirill Savostyanov, Alexander Pushkov et Dmitry Sladkov. « GP76 Experience in treatment of bladder exstrophy in newborn girl with apert syndrome ». Dans Faculty of Paediatrics of the Royal College of Physicians of Ireland, 9th Europaediatrics Congress, 13–15 June, Dublin, Ireland 2019. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2019. http://dx.doi.org/10.1136/archdischild-2019-epa.142.

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Rapports d'organisations sur le sujet "EXSTROPHY"

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Stuhldreher, Peter, et John Gearhart. Modern staged repair of bladder exstrophy. BJUI Knowledge, septembre 2019. http://dx.doi.org/10.18591/bjuik.0243.

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Deshpande, Aniruddh, et Naeem Samnakay. Long term outcomes of bladder exstrophy and their implications. BJUI Knowledge, novembre 2021. http://dx.doi.org/10.18591/bjuik.0222.v2.

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Principles of neonatal bladder exstrophy management. BJUI Knowledge, octobre 2017. http://dx.doi.org/10.18591/bjuik.0220.

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Long term outcomes of bladder exstrophy and their implications. BJUI Knowledge, janvier 2016. http://dx.doi.org/10.18591/bjuik.0222.

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