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In humans, penile agenesis is an extremely rare congenital condition. It is thought to occur once per 5-10 million births and is characterized by the male child's lack of a penis at birth. Although it was previously thought that there were fewer occurrences, recent study has revealed that the sickness is significantly more prevalent in India and Southeast Asia. The majority of patients have no known family history of aphalia and generally have normal male anatomy, with the exception of the lack of a penis.