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Penis, bladder and uretral agenesis associated with anorectal malformation in a living male neonate. Case report.
Clin Exp Obstet Gynecol. 1999; 26(3-4):225-6.CE

Abstract

Aphallia is a very rare congenital malformation, with an occurrence of 1 in every 30 million births. In the international literature about 75 cases have been indicated as of today. The authors report and discuss the case of one neonate, born from a monoamniotic twin delivery, suffering from agenesis of the penis, anorectal malformation with a fully formed scrotum with 2 normal gonads and absence of bladder and urethra and both kidneys.

Authors+Show Affiliations

Department of Pediatric Surgery, Catania University, Italy.No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

10668164

Citation

Di Benedetto, V, et al. "Penis, Bladder and Uretral Agenesis Associated With Anorectal Malformation in a Living Male Neonate. Case Report." Clinical and Experimental Obstetrics & Gynecology, vol. 26, no. 3-4, 1999, pp. 225-6.
Di Benedetto V, Idotta R, Lebet M, et al. Penis, bladder and uretral agenesis associated with anorectal malformation in a living male neonate. Case report. Clin Exp Obstet Gynecol. 1999;26(3-4):225-6.
Di Benedetto, V., Idotta, R., Lebet, M., & Puntorieri, A. (1999). Penis, bladder and uretral agenesis associated with anorectal malformation in a living male neonate. Case report. Clinical and Experimental Obstetrics & Gynecology, 26(3-4), 225-6.
Di Benedetto V, et al. Penis, Bladder and Uretral Agenesis Associated With Anorectal Malformation in a Living Male Neonate. Case Report. Clin Exp Obstet Gynecol. 1999;26(3-4):225-6. PubMed PMID: 10668164.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Penis, bladder and uretral agenesis associated with anorectal malformation in a living male neonate. Case report. AU - Di Benedetto,V, AU - Idotta,R, AU - Lebet,M, AU - Puntorieri,A, PY - 2000/2/11/pubmed PY - 2000/3/4/medline PY - 2000/2/11/entrez SP - 225 EP - 6 JF - Clinical and experimental obstetrics & gynecology JO - Clin Exp Obstet Gynecol VL - 26 IS - 3-4 N2 - Aphallia is a very rare congenital malformation, with an occurrence of 1 in every 30 million births. In the international literature about 75 cases have been indicated as of today. The authors report and discuss the case of one neonate, born from a monoamniotic twin delivery, suffering from agenesis of the penis, anorectal malformation with a fully formed scrotum with 2 normal gonads and absence of bladder and urethra and both kidneys. SN - 0390-6663 UR - https://www.unboundmedicine.com/medline/citation/10668164/Penis_bladder_and_uretral_agenesis_associated_with_anorectal_malformation_in_a_living_male_neonate__Case_report_ L2 - http://www.diseaseinfosearch.org/result/5659 DB - PRIME DP - Unbound Medicine ER -