Penile agenesis: Difference between revisions
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==Overview== | ==Overview== | ||
'''Penile agenesis''' is a very rare [[birth defect]] in [[human]]s, occurring about once in 5-10 million births, where a male child is born without a [[penis]].<ref>{{cite journal|last=Bangroo|first=A. K.|coauthors=Ramji Khetri and Shashi Tiwari|date=2005|title=Penile agenesis|journal=J. Indian Assoc. Pediatr. Surg.|volume=10|issue=4|url=http://medind.nic.in/jan/t05/i4/jant05i4p256.pdf}}</ref> There were recently thought to be fewer but the condition is remarkably more frequent in India and South-east Asia. It is also known as [[aphallia]] [from the Greek, "a" for negative or no, and "phallia" for penis]. Most patients have no known family history of aphallia, and often have a normal male anatomy, save for the absence of the penis. | |||
A partner condition is testicular or gonadal agenesis. This is where the male child is born without [[gonads]] and consequently develops no [[testes]]. The function of [[Leydig cells]] in the [[embryo]] is to convert the gonads into [[testicles]] in males-to-be and into [[ovaries]] in females. In this condition, the process fails. | |||
Penile agenesis can exist independently after full testicular development, though the causes of this in particular are uncertain. Testes are the sole producer of [[5-alpha dihydrotestosterone]] (5aDHT) in the male body. One cause of the gonads failing to metamorphose into testes is the absence of 5aDHT. Therefore the masculizing process to allow for the development of the genital tubercle which eventually becomes the penis is halted. In this scenario, the child is born with penile and testicular agenesis. Another slang term for this condition is "nullo". | |||
The sufferers of just one of the conditions usually continue as males throughout their lives. With very few exceptions the penile and testicular agenetic is brought up as a female and eventually undergoes http://www.wikidoc.org/index.php/Sex_reassignment_surgery. This is despite being 46xy karyotype male and having no female sexual characteristics. This is an unclear part of anatomy. The organs that prevent the development of the embryo into a female are called [[Anti-Mullerian hormones]]. They are commonly believed to be created in the testes, but male embryos without testes still appear to produce these hormones. | |||
==Complications== | |||
One complication of the full condition is the absence of a urinary outlet. This can be approached as follows. Before genital metamorphosis, the [[urethra]] runs down the anal wall, to be pulled away by the genital tubercle during male development. It remains there in the agenetic. In one case, 45 years ago, the surgeons redirected the urethra to the rim of the [[anus]] immediately after birth. | |||
Patients with penile and testicular agenesis are [[impotent]]. | |||
==Treatment== | |||
Largely, treatment is psychological and surgical reconstruction. | |||
== See also == | ==See also== | ||
*[[Agenesis]] | *[[Agenesis]] | ||
*[[Diphallia]] | *[[Diphallia]] | ||
{{ | ==References== | ||
{{reflist|2}} | |||
{{Congenital malformations of genital organs and urinary system}} | |||
{{WH}} | {{WH}} | ||
{{WikiDoc Sources}} | {{WikiDoc Sources}} | ||
[[Category:Disease]] | |||
Latest revision as of 13:45, 6 September 2012
| Penile agenesis | |
| ICD-9 | 752.69 |
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Overview
Penile agenesis is a very rare birth defect in humans, occurring about once in 5-10 million births, where a male child is born without a penis.[1] There were recently thought to be fewer but the condition is remarkably more frequent in India and South-east Asia. It is also known as aphallia [from the Greek, "a" for negative or no, and "phallia" for penis]. Most patients have no known family history of aphallia, and often have a normal male anatomy, save for the absence of the penis.
A partner condition is testicular or gonadal agenesis. This is where the male child is born without gonads and consequently develops no testes. The function of Leydig cells in the embryo is to convert the gonads into testicles in males-to-be and into ovaries in females. In this condition, the process fails.
Penile agenesis can exist independently after full testicular development, though the causes of this in particular are uncertain. Testes are the sole producer of 5-alpha dihydrotestosterone (5aDHT) in the male body. One cause of the gonads failing to metamorphose into testes is the absence of 5aDHT. Therefore the masculizing process to allow for the development of the genital tubercle which eventually becomes the penis is halted. In this scenario, the child is born with penile and testicular agenesis. Another slang term for this condition is "nullo".
The sufferers of just one of the conditions usually continue as males throughout their lives. With very few exceptions the penile and testicular agenetic is brought up as a female and eventually undergoes http://www.wikidoc.org/index.php/Sex_reassignment_surgery. This is despite being 46xy karyotype male and having no female sexual characteristics. This is an unclear part of anatomy. The organs that prevent the development of the embryo into a female are called Anti-Mullerian hormones. They are commonly believed to be created in the testes, but male embryos without testes still appear to produce these hormones.
Complications
One complication of the full condition is the absence of a urinary outlet. This can be approached as follows. Before genital metamorphosis, the urethra runs down the anal wall, to be pulled away by the genital tubercle during male development. It remains there in the agenetic. In one case, 45 years ago, the surgeons redirected the urethra to the rim of the anus immediately after birth.
Patients with penile and testicular agenesis are impotent.
Treatment
Largely, treatment is psychological and surgical reconstruction.
See also
References
- ↑ Bangroo, A. K. (2005). "Penile agenesis" (PDF). J. Indian Assoc. Pediatr. Surg. 10 (4). Unknown parameter
|coauthors=ignored (help)