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[Anorectal malformations].
Arch Pediatr. 2013 Sep; 20 Suppl 1:S19-27.AP

Abstract

Anorectal malformations (ARM) are the result of an abnormal development of the terminal part of the digestive tract interesting anus and/or rectum that occur early between the sixth and tenth week of embryonic development. They carry a malformation spectrum of severity depending on the level of disruption of the anorectal canal and of the associated caudal malformations (sacrum and spine). ARM are associated in over half the cases with other malformations that can be integrated in some cases in known syndromes. If surgical treatment to restore anatomy as normal as possible is indispensable, post-operative care is essential for these patients whose defecation mechanisms are altered, to reach if not continence, at least a socially acceptable cleanliness.

Authors+Show Affiliations

Service de Chirurgie pédiatrique, CRMR Malformations ano-rectales et pelviennes rares (MAREP), Hôpital Necker Enfants Malades, Université Paris Descartes, 149 rue de Sèvres, 75015 Paris, France.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

fre

PubMed ID

23992833

Citation

Cretolle, C, et al. "[Anorectal Malformations]." Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie, vol. 20 Suppl 1, 2013, pp. S19-27.
Cretolle C, Rousseau V, Lottmann H, et al. [Anorectal malformations]. Arch Pediatr. 2013;20 Suppl 1:S19-27.
Cretolle, C., Rousseau, V., Lottmann, H., Irtan, S., Lortat-Jacob, S., Alova, I., Michel, J. L., Aigrain, Y., Podevin, G., Lehur, P. A., & Sarnacki, S. (2013). [Anorectal malformations]. Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie, 20 Suppl 1, S19-27. https://doi.org/10.1016/S0929-693X(13)71405-2
Cretolle C, et al. [Anorectal Malformations]. Arch Pediatr. 2013;20 Suppl 1:S19-27. PubMed PMID: 23992833.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Anorectal malformations]. AU - Cretolle,C, AU - Rousseau,V, AU - Lottmann,H, AU - Irtan,S, AU - Lortat-Jacob,S, AU - Alova,I, AU - Michel,J L, AU - Aigrain,Y, AU - Podevin,G, AU - Lehur,P A, AU - Sarnacki,S, PY - 2013/9/3/entrez PY - 2013/9/3/pubmed PY - 2014/5/3/medline SP - S19 EP - 27 JF - Archives de pediatrie : organe officiel de la Societe francaise de pediatrie JO - Arch Pediatr VL - 20 Suppl 1 N2 - Anorectal malformations (ARM) are the result of an abnormal development of the terminal part of the digestive tract interesting anus and/or rectum that occur early between the sixth and tenth week of embryonic development. They carry a malformation spectrum of severity depending on the level of disruption of the anorectal canal and of the associated caudal malformations (sacrum and spine). ARM are associated in over half the cases with other malformations that can be integrated in some cases in known syndromes. If surgical treatment to restore anatomy as normal as possible is indispensable, post-operative care is essential for these patients whose defecation mechanisms are altered, to reach if not continence, at least a socially acceptable cleanliness. SN - 1769-664X UR - https://www.unboundmedicine.com/medline/citation/23992833/[Anorectal_malformations]_ DB - PRIME DP - Unbound Medicine ER -