Penile Agenesis Associated with Anorectal Malformation and Bilateral Renal Agenesis: A Case Report and a Review of the Literature.

Bibliographic Details
Title: Penile Agenesis Associated with Anorectal Malformation and Bilateral Renal Agenesis: A Case Report and a Review of the Literature.
Authors: Adumah, Collins Chijioke, Akpaette, Iniofon Clement, Oni, Owolabi, Obasi, Igwe Arua, Ogundele, Ibukunolu Olufemi, Adesunkanmi, Abdulhafiz, Oyinloye, Oluwaseun Abioye, Talabi, Ademola Olusegun, Sowande, Oludayo Adedapo, Adejuyigbe, Olusanya
Source: African Journal of Paediatric Surgery; Jan-Mar2024, Vol. 21 Issue 1, p75-77, 3p
Subject Terms: MASCULINE identity, HUMAN abnormalities, AGENESIS of corpus callosum, GENOTYPES, PENIS
Abstract: Penile agenesis is complete absence of the penis in an otherwise normal phenotypic and genotypic male at birth that results from failure of development of the genital tubercle. It is an extremely rare anomaly that may be associated with anomalies in other organ systems, the extent and severity of which may affect the prognosis. The management is challenging and may have far reaching implications for the individual and family. While gender reassignment with bilateral orchidectomy and feminising genitoplasty has been carried out for most patients, significant psychosexual and social issues related to the male identity may occur due to foetal or postnatal sex steroid imprinting. We report a neonate with penile agenesis with bilateral renal agenesis and anorectal malformation. [ABSTRACT FROM AUTHOR]
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  Data: Penile Agenesis Associated with Anorectal Malformation and Bilateral Renal Agenesis: A Case Report and a Review of the Literature.
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  Data: <searchLink fieldCode="AR" term="%22Adumah%2C+Collins+Chijioke%22">Adumah, Collins Chijioke</searchLink><br /><searchLink fieldCode="AR" term="%22Akpaette%2C+Iniofon+Clement%22">Akpaette, Iniofon Clement</searchLink><br /><searchLink fieldCode="AR" term="%22Oni%2C+Owolabi%22">Oni, Owolabi</searchLink><br /><searchLink fieldCode="AR" term="%22Obasi%2C+Igwe+Arua%22">Obasi, Igwe Arua</searchLink><br /><searchLink fieldCode="AR" term="%22Ogundele%2C+Ibukunolu+Olufemi%22">Ogundele, Ibukunolu Olufemi</searchLink><br /><searchLink fieldCode="AR" term="%22Adesunkanmi%2C+Abdulhafiz%22">Adesunkanmi, Abdulhafiz</searchLink><br /><searchLink fieldCode="AR" term="%22Oyinloye%2C+Oluwaseun+Abioye%22">Oyinloye, Oluwaseun Abioye</searchLink><br /><searchLink fieldCode="AR" term="%22Talabi%2C+Ademola+Olusegun%22">Talabi, Ademola Olusegun</searchLink><br /><searchLink fieldCode="AR" term="%22Sowande%2C+Oludayo+Adedapo%22">Sowande, Oludayo Adedapo</searchLink><br /><searchLink fieldCode="AR" term="%22Adejuyigbe%2C+Olusanya%22">Adejuyigbe, Olusanya</searchLink>
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  Data: African Journal of Paediatric Surgery; Jan-Mar2024, Vol. 21 Issue 1, p75-77, 3p
– Name: Subject
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  Data: <searchLink fieldCode="DE" term="%22MASCULINE+identity%22">MASCULINE identity</searchLink><br /><searchLink fieldCode="DE" term="%22HUMAN+abnormalities%22">HUMAN abnormalities</searchLink><br /><searchLink fieldCode="DE" term="%22AGENESIS+of+corpus+callosum%22">AGENESIS of corpus callosum</searchLink><br /><searchLink fieldCode="DE" term="%22GENOTYPES%22">GENOTYPES</searchLink><br /><searchLink fieldCode="DE" term="%22PENIS%22">PENIS</searchLink>
– Name: Abstract
  Label: Abstract
  Group: Ab
  Data: Penile agenesis is complete absence of the penis in an otherwise normal phenotypic and genotypic male at birth that results from failure of development of the genital tubercle. It is an extremely rare anomaly that may be associated with anomalies in other organ systems, the extent and severity of which may affect the prognosis. The management is challenging and may have far reaching implications for the individual and family. While gender reassignment with bilateral orchidectomy and feminising genitoplasty has been carried out for most patients, significant psychosexual and social issues related to the male identity may occur due to foetal or postnatal sex steroid imprinting. We report a neonate with penile agenesis with bilateral renal agenesis and anorectal malformation. [ABSTRACT FROM AUTHOR]
– Name: Abstract
  Label:
  Group: Ab
  Data: <i>Copyright of African Journal of Paediatric Surgery is the property of Wolters Kluwer India Pvt Ltd and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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        Value: 10.4103/ajps.ajps_81_22
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      – Code: eng
        Text: English
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    Subjects:
      – SubjectFull: MASCULINE identity
        Type: general
      – SubjectFull: HUMAN abnormalities
        Type: general
      – SubjectFull: AGENESIS of corpus callosum
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      – SubjectFull: GENOTYPES
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      – SubjectFull: PENIS
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      – TitleFull: Penile Agenesis Associated with Anorectal Malformation and Bilateral Renal Agenesis: A Case Report and a Review of the Literature.
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              M: 01
              Text: Jan-Mar2024
              Type: published
              Y: 2024
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