Aphallia Support

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Aphallia Intersex Society of North America

    https://isna.org/faq/conditions/aphalia
    The Intersex Society of North America closed its doors and stopped updating this website in 2008. ISNA’s work is continued by interACT: Advocates for Intersex Youth, who proudly preserves this website as a historical archive.For current information, links to intersex support groups, and to connect with intersex advocates, please head to interACT: Advocates for Intersex Youth.

Aphallia: Report of three cases and literature review

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918779/
    Aphallia or penile agenesis is a rare malformation accompanying with no phallus. This anomaly is extremely rare with abnormality of urogenital system and psychological consequences. Its outbreak is estimated 1 out of 10-30 million births.Reviewing 3 cases ...Cited by: 1

Diphallus and Aphallia - American Urological Association

    https://www.auanet.org/education/auauniversity/education-products-and-resources/pathology-for-urologists/penis/congenital/anatomical-defects/diphallus-and-aphallia
    Welcome to the updated version of Pathology for Urologists! This program was designed to help Urology residents and fellows familiarize themselves with the pathologic features of common urologic entities. This will serve not only as a resource tool for your review but …

Aphallia in an adult male with 46,XY karyotype - Wang ...

    https://onlinelibrary.wiley.com/doi/full/10.1111/j.1442-2042.2011.02785.x
    Aphallia is a rare urogenital anomaly with an estimated incidence of 1 in 10–30 million. We report a case of aphallia in a male, who had two well‐developed testicles, but lacked a penis. Digital rectal examination revealed the urethral meatus was opening to the anterior wall of the rectum posterior to the sphincter.Cited by: 4

Aphallia in an adult Paul Ekka NM, Malua S, Bodra P, Jha ...

    http://www.archintsurg.org/article.asp?issn=2278-9596;year=2015;volume=5;issue=3;spage=181;epage=183;aulast=Paul
    Aphallia should be differentiated from concealed penis, rudimentary penis, micropenis, male pseudohermaphroditism and intrauterine amputation of the penis. The recommended surgical treatment for patients with aphallia, presenting in infancy, is early sex assignment to the female gender.Author: Nishith M Paul Ekka, Shital Malua, Pankaj Bodra, Rohit Kumar Jha

Portland Aphasia Support Group - National Aphasia Association

    https://www.aphasia.org/site/portland-aphasia-support-group/
    *Meets 1st and 3rd Thurday from 3:15PM-5PM. Aphasia Spouse Support Group ...

Aphallia: Case report and review of the literature Kumar A ...

    http://www.saudisurgj.org/article.asp?issn=2320-3846;year=2015;volume=3;issue=1;spage=13;epage=16;aulast=Kumar;type=3
    Mar 23, 2015 · Aphallia or absence of the penis is a very rare congenital anomaly with an estimated incidence of 1 in 10,000,000 births. A total of about 80 cases have been documented so far. We present a case of 1-day neonate who was born preterm at 30 weeks by normal vaginal delivery with a …Author: Amarendra Kumar, Nameer Faiz

A rare case of penis agenesis (Aphallia) with associated ...

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4601949/
    Aug 10, 2015 · 1. Introduction. The penis agenesis (PA) is an extremely rare genitourinary anomaly with an incidence of about one in 30 million births .It is believed to result from the absence or a failure in the development of genital tubercule .Since it was originally described by Imminger in 1853, approximately 100 cases have been described worldwide.Cited by: 1

Aphallia - Wikipedia

    https://en.wikipedia.org/wiki/Aphallia
    Aphallia is a congenital malformation in which the phallus (penis or clitoris) is absent.It is the female counterpart of penile agenesis and testicular agenesis. The word is derived from the Greek a-for "not", and phallos for "penis". It is classified as an intersex condition.Other names: Penile agenesis

Life with Achalasia

    https://lifewithachalasia.blogspot.com/
    Jun 04, 2012 · Both sites though helped me feel like I was not alone in my battle with this condition or disease of Achalasia. My plan for this blog is to chronically record my Life with Achalasia. I hope and pray that some will find this blog helpful and informative as they deal with Achalasia in their own lives or the lives of loved ones they support.



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