Diphallia

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Diphallia
Diphallia 01.jpg
Synonyms Penile duplication
Pronounce N/A
Specialty N/A
Symptoms Presence of two penises
Complications Urinary tract infection, erectile dysfunction, infertility
Onset Congenital
Duration Lifelong
Types N/A
Causes Genetic mutation, developmental anomaly
Risks Hypospadias, bladder exstrophy, anorectal malformations
Diagnosis Physical examination, imaging studies
Differential diagnosis Hypospadias, epispadias, bladder exstrophy
Prevention None
Treatment Surgical intervention
Medication N/A
Prognosis Variable, depends on associated anomalies
Frequency 1 in 5-6 million live births
Deaths N/A


A rare congenital condition characterized by the presence of two penises


Diphallia, also known as penile duplication, is a rare congenital condition in which a male is born with two penises. This anomaly was first reported in 1609 by the Swiss physician Johannes Jacob Wecker. The condition is extremely rare, with an estimated occurrence of 1 in 5 to 6 million live births.

Etiology[edit | edit source]

The exact cause of diphallia is not well understood, but it is believed to occur during the early stages of embryonic development. It is thought to result from an abnormality in the cloacal membrane during the fourth to sixth weeks of gestation. Genetic factors, environmental influences, and teratogenic agents may contribute to the development of this condition.

Classification[edit | edit source]

Diphallia can be classified into two main types:

  • Complete diphallia: Both penises are fully developed and functional.
  • Partial diphallia: One of the penises is smaller or underdeveloped.

Associated Anomalies[edit | edit source]

Diphallia is often associated with other congenital anomalies, including:

Diagnosis[edit | edit source]

Diagnosis of diphallia is typically made at birth through physical examination. Further evaluation may include imaging studies such as ultrasound, MRI, or CT scan to assess the extent of duplication and associated anomalies.

Management[edit | edit source]

The management of diphallia depends on the type and severity of the condition, as well as the presence of associated anomalies. Surgical intervention is often required to correct functional and cosmetic issues. The goals of surgery may include:

  • Removal of the less functional or smaller penis
  • Reconstruction of the urethra
  • Correction of associated anomalies

Prognosis[edit | edit source]

The prognosis for individuals with diphallia varies depending on the severity of the condition and the presence of associated anomalies. With appropriate surgical management, many individuals can lead normal lives.

See also[edit | edit source]

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Contributors: Prab R. Tumpati, MD