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Aphallia: A Very Rare Congenital Anomaly, With Associated Genitourinary And Ano-Rectal Malformation.
J Ayub Med Coll Abbottabad. 2018 Apr-Jun; 30(2):275-277.JA

Abstract

Aphallia or penile agenesis is very rare congenital anomaly of unknown cause occurring 1 in 30 million live births. Very little has been written in literature about aphallia. There is absent phallus and urethra may open abnormally in perineum or into rectum posing various surgical, social and psychological implications as the child grows. We are presenting 03 cases of aphallia with associated congenital anomalies such as unilateral renal agenesis, bilateral undescended testes, anorectal malformation and rectovasical fistula.

Authors+Show Affiliations

Department of Paediatric Surgery, Children Hospital, PIMS, Islamabad, Pakistan.Department of Paediatric Surgery, Children Hospital, PIMS, Islamabad, Pakistan.Department of Paediatric Surgery, Children Hospital, PIMS, Islamabad, Pakistan.PAEC General Hospital, Islamabad, Pakistan.Rawalpindi Medical College, Pakistan.

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

29938433

Citation

Nisar, Muhammad Umar, et al. "Aphallia: a Very Rare Congenital Anomaly, With Associated Genitourinary and Ano-Rectal Malformation." Journal of Ayub Medical College, Abbottabad : JAMC, vol. 30, no. 2, 2018, pp. 275-277.
Nisar MU, Akhtar N, Gondal MF, et al. Aphallia: A Very Rare Congenital Anomaly, With Associated Genitourinary And Ano-Rectal Malformation. J Ayub Med Coll Abbottabad. 2018;30(2):275-277.
Nisar, M. U., Akhtar, N., Gondal, M. F., Sikander, S., & Viqar, S. (2018). Aphallia: A Very Rare Congenital Anomaly, With Associated Genitourinary And Ano-Rectal Malformation. Journal of Ayub Medical College, Abbottabad : JAMC, 30(2), 275-277.
Nisar MU, et al. Aphallia: a Very Rare Congenital Anomaly, With Associated Genitourinary and Ano-Rectal Malformation. J Ayub Med Coll Abbottabad. 2018 Apr-Jun;30(2):275-277. PubMed PMID: 29938433.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Aphallia: A Very Rare Congenital Anomaly, With Associated Genitourinary And Ano-Rectal Malformation. AU - Nisar,Muhammad Umar, AU - Akhtar,Nadeem, AU - Gondal,Mudassar Fiaz, AU - Sikander,Samer, AU - Viqar,Sana, PY - 2018/6/26/entrez PY - 2018/6/26/pubmed PY - 2018/10/16/medline KW - Absent penis KW - Ambiguous genetalia KW - Aphallia KW - Neophallusn KW - Penile agenesis KW - Penile reconstruction KW - Phalloplasty SP - 275 EP - 277 JF - Journal of Ayub Medical College, Abbottabad : JAMC JO - J Ayub Med Coll Abbottabad VL - 30 IS - 2 N2 - Aphallia or penile agenesis is very rare congenital anomaly of unknown cause occurring 1 in 30 million live births. Very little has been written in literature about aphallia. There is absent phallus and urethra may open abnormally in perineum or into rectum posing various surgical, social and psychological implications as the child grows. We are presenting 03 cases of aphallia with associated congenital anomalies such as unilateral renal agenesis, bilateral undescended testes, anorectal malformation and rectovasical fistula. SN - 1819-2718 UR - https://www.unboundmedicine.com/medline/citation/29938433/Aphallia:_A_Very_Rare_Congenital_Anomaly_With_Associated_Genitourinary_And_Ano_Rectal_Malformation_ L2 - http://jamc.ayubmed.edu.pk/index.php/jamc/article/view/xxxxx DB - PRIME DP - Unbound Medicine ER -