Pakistan Baby Born With Double Penises & No Anus — Rare Case of Diphallia
An infant in Pakistan born with two penises and no anus — a rare diphallia case affecting roughly 1 in 5–6 million births, requiring immediate surgical care.
Pakistan Baby Born With Double Penises & No Anus – Rare ‘One In Six Million’ Diphallia Disorder Shocks Medical Experts
A shocking and extremely rare medical case has emerged from Pakistan where a newborn baby boy was born with two fully developed penises and no anus. The condition, known as diphallia, is one of the rarest congenital disorders recorded in medical science and reportedly occurs in only one out of every six million live births. The baby could urinate through both penises, but the absence of an anal opening created a life-threatening emergency that required immediate surgery.
Doctors noted that both organs were functioning, with the larger measuring around 2.5 cm and the smaller 1.5 cm. Because the infant could not pass stool naturally, surgeons performed an urgent colostomy to create an alternate opening, allowing waste to leave the body safely.
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Understanding Diphallia: The Rare Double-Penis Disorder
Diphallia, also known as penile duplication, was first documented more than 400 years ago, and only around 100 similar cases have been medically recorded since then. The condition appears in different forms: some infants have partial duplication, while others are born with two complete and functional penises. Many children with diphallia are also born with additional abnormalities, often involving the bladder, kidneys, colon, or spine. Because each case differs significantly, doctors must design a personalized treatment plan for every affected child.
How Does Diphallia Occur?
Medical researchers believe diphallia develops during the early weeks of fetal growth, typically between the third and sixth week of pregnancy. At this stage, the genital tubercle divides abnormally or duplicates, possibly due to disruptions in embryonic tissue development. This duplication can also affect nearby organs such as the colon or urinary tract, explaining why many diphallia cases include complications such as missing anus, malformed kidneys, or urethral abnormalities.
Scientists still do not know the exact cause of diphallia. There are no confirmed genetic causes or environmental triggers, and cases appear to occur randomly without identifiable risk factors.
The Surgical Decision: Removing the Bigger Penis
After examining the newborn’s anatomy, doctors discovered that both penises contained their own urethra, but both were connected to a single bladder. In cases like this, surgeons typically remove the organ that is less functional or poorly positioned. Surprisingly, in this instance the larger penis was removed because the smaller one had better positioning to support natural urination.
The surgery was successful, and the infant is reported to be in stable condition. Additional procedures will be required in the future, particularly to construct a permanent anal opening once the baby is strong enough to undergo further operations.
Long-Term Health and Life Challenges
Children with severe congenital abnormalities like diphallia often require lifelong medical monitoring. Possible challenges may include urinary complications, multiple corrective surgeries, fertility concerns later in life, and emotional adjustments during adolescence and adulthood. Despite the complexity, many individuals with diphallia have reportedly grown up to lead normal, healthy lives with the help of surgical reconstruction and family support.
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A Case That Raises Awareness and Ethical Questions
The Pakistan Baby Born With Double Penises & No Anus is a medical rarity that highlights the limits and strengths of modern medicine. Surgeons must make decisions that will shape the child’s entire future, balancing functionality, physical health, and psychological well-being.
While the case is shocking, it also raises awareness about rare birth defects and the importance of advanced neonatal care. It reminds the world of the resilience of newborns and the evolving capabilities of pediatric surgery in giving affected children a chance at a healthy life.
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