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    It is thought diphallia occurs in the fetus between the 23rd and 25th days of gestation when an injury, chemical stress, or malfunctioning homeobox genes hamper proper function of the caudal cell mass of the fetal mesoderm as the urogenital sinus separates from the genital tubercle and rectum to form the penis.

    The first case was reported by Wecker in Bologna, Italy in , and since then, about one hundred cases have been reported until today. According to Schneider classification in , double penis is classified into three groups: a glans diphallia, b bifid diphallia and c complete diphallia or double penis.

    The current widely accepted classification, introduced by Aleem in , classifies double penis into two groups: true diphallia and bifid phallus.

    Diphallia is usually accompanied by systemic anomalies, their extent varies, ranging from no associated anomaly to multiple anomalies including urogenital, gastrointestinal and musculoskeletal systems.

    A 2-day old male newborn, [6] associated with complex genitourinary and ano-rectal malformation. He had imperforated anus, hypospadias , bifid scrotum, meatuses on both glandes, two bladders and two colons , and had typical testes , kidneys and ureters.

    Refer Figure 3. Partial true diphallia corresponds to pseudodiphallia. The small, immature and nonfunctional penis protruded on one side of the large, normal penis.

    The secondary penis had glans but without urinary meatus. Refer Figure 1. A year-old boy, [1] associated with bifid scrotum , epispadia and pubic symphysis diastasis.

    He had two separate penises, similar in size and shape, each penis had an epispadia urethral meatus. He had bifid scrotum, one testicle on each side of the scrotum.

    A bowel loop-like structure was over the pubis region. This structure had no communication with any other structures.

    He had a single normal bladder and ureter. Refer Figure 2. A year-old boy, [14] apart from having two penises, had normal external genitalia.

    His two testicles were within normal scrotum and normally positioned. He had two unequal sized glandes at tip of a thick penile shaft , and only urinated through the larger glans.

    He had a patent anus, one bladder, one typical urethra, typical gastrointestinal and genitourinary systems. Refer Figure 4.

    A male typically inherits an X chromosome from ovum and a Y chromosome from spermatozoon. The presence of the sex-determining-region of the Y chromosome, or SRY gene , determines the embryo being a male.

    Internal and external male genitalia development from bipotential gonad in embryo. Initial development of external genital is independent of androgens before indifferent gonads differentiate into testes.

    External genitalia develop from mesenchymal cells underlying coelomic epithelium lining urogenital ridges on posterior wall of abdomen.

    Hormone—dependent development of external genitalia begins at about week eight. DHT causes development of other male sex characteristics, such as prostate development, differentiation of external genitalia including genital tubercle elongation forming glans penis, urogenital folds forming penile shaft and labioscrotal swellings forming scrotum by week ten.

    Cause of diphallia is unknown, [13] and also because its associated anomalies vary largely, it is impossible to give a simple, single explanation of its cause.

    Normal development of penis occurs with the fusion of cloacal tubercles at anterior end of urogenital sinus. Diphallia is a rare abnormal external genitalia.

    The cause is uncertain, but most scientists agree that diphallia is a defect of genital tubercle, and occurs at about week three of gestation, when caudal cell mass of mesoderm is affected by various external environmental factors including drugs, infections and malfunctioning homeobox genes.

    Treatment is a case-by-case analysis taking into account considerations for medical and ethical reasons, and involves surgical excision of the non-functioning penis.

    From Wikipedia, the free encyclopedia. Diphallia Diphallia Diphallia , penile duplication PD , diphallic terata , or diphallasparatus , is an extremely rare developmental abnormality in which a person is born with two penises.

    About a year ago, he did an AMA on Reddit , that turned out to be one of the most popular of all time. It was revealed that DiphallicDude is bisexual, and has had sex with over people.

    It has been holding the title of 1 Bestseller for Kindle in 3 different categories. All of the sexy details left out of the AMA have been described in the book, in addition to all of the other ways diphallia has affected his life.

    Recently, he gave an interview with BBC Newsbeat , discussing what it was like growing up. His parents cautioned him to keep his condition private and not tell other children.

    When he was in high school, he actually considered having one of the penises removed. This website uses cookies to improve user experience.

    By continuing to use our website you consent to all cookies in accordance with our cookie policy. Share on Facebook.

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