Long before the concept of "designer babies" created in a lab became the stuff of science fiction, inbreeding in royal families was viewed as a way to ensure genetic purity. Intermarriage ensured that no "common" blood sullied pure, aristocratic blood lines. What could go wrong?
A lot, actually. Birth defects caused by inbreeding were rampant in royal families from Russia to Portugal and even in ancient Egypt, where the practice of sibling marriage was considered godly behavior. Hereditary diseases caused by inbreeding get handed down through thin gene pools, particularly in the many cases where intentional close marriage is used to ensured that royal blood (and its recurrent flaws) are kept in the family. For example, Queen Victoria, a major proponent of pure blood lines, married her cousin Albert, and the two had nine children who then passed hemophilia to royal families throughout Europe. Both King Tut and Charles II of Spain were so deformed by inbreeding that they were unable to walk unaided. Meanwhile, mental illnesses ran rampant throughout many royal families, leading to some very odd royal behavior.
While all these families hoped close intermarriage would keep their royal families stronger, in many cases, illness, madness, and infertility caused by inbreeding wound up tearing them apart.
Of all the inbred royals, Charles II of Spain won top prize for being obviously hindered by his hereditary traits. The product of a long line of Habsburg inbreeding (his father and mother were uncle and niece), Charles II (nicknamed "The Bewitched") looked the part. He had what was called the Habsburg Jaw or Habsburg Lip, characterized by a huge tongue, an under-bite, a jutting lower jaw, and a thick lower lip. Technically, the deformity is known as mandibular prognathism. His tongue made it difficult to chew and caused excessive drooling.
The king was also severely developmentally delayed. He was breastfed until he was five, and never received any formal education. His speech was delayed until he was four, and he couldn’t walk until the age of eight. Even as an adult, his communication was muffled and hardly comprehensible. He was also impotent, so his inability to procreate ended the Habsburg’s hold on the Spanish crown when the king died at age 39 in 1700.
The Habsburg dynasty had been intermarrying for so long that one of Charles's ancestors, Joanna of Castille, appears in his family tree 14 different times. In fact, Charles I was more inbred than he would have been if his parents had been brother and sister.
Tsarevich Alexei Nikolaevich's hemophilia contributed to the fall of the Russia imperial dynasty in 1917. While no one in the ruling Russian House of Romanov was known to carry hemophilia (a potentially fatal genetic disease where blood does not clot normally), Alexei's father Tsar Nicholas had married into the family of Queen Victoria of England, who was part of clan of passionate inbreeds. Tsarist Alexandra was Victoria's granddaughter.
Desperate to save her son's life, Alexandra sought mystical intervention in the form of Rasputin, the "Mad Monk.” Inviting a lascivious man like Rasputin, known for his tastes for alcohol and lovers of both genders, didn’t go over well with the aristocracy. The Russian rulers, however, were convinced that Rasputin’s treatments were effective in saving their son.
The mystic Rasputin gained greater influence at court, wielding increasing power over the lives of the royals and surreptitiously governing Russia. The disorder in the royal house and the questionable company the rulers kept helped spur the Russian Revolution of 1917, and as a result, the entire royal family was executed.
Nor was Alexei the only relative of Queen Victoria's to be afflicted with hemophilia:
"The 19th century British monarch's son Leopold, Duke of Albany, died from blood loss after he slipped and fell. Her grandson Friedrich bled out at age 2; her grandsons Leopold and Maurice, at ages 32 and 23, respectively."
Age: 14 (1904-1918)
Birthplace: Petergofsee more on Alexei Nikolaevich, Tsarevich of Russia
Although his legacy is as the golden boy pharaoh of ancient Egypt, DNA tests of King Tut's mummified corpse show that this ruler of Egypt circa 1300 BC was actually a feeble-bodied genetic misfit, owing to the Egyptian royal tradition of brothers and sisters marrying one another. King Tutankhamun took the throne at age 10 and survived only until the age of 19. He likely had a cleft palate, a club foot, and scoliosis, as well as an elongated, deformed skull. He probably required a cane to walk and evidence suggests he suffered from malaria because of a weak immune system.
Egyptian pharaohs revered sibling marriage, influenced by the legend that the god Osiris married his sister, Isis, to maintain a pure bloodline. There were even instances of "double niece" marriages (defined as when a man marries a girl who was the offspring of his brother and sister).
King George III of England, whose reign was famously marked by losing the American Revolution, likely had a genetic disorder that affected his mind more noticeably than his body. He is a believed to have suffered from porphyria, a disease that makes a patient’s urine bluish purple and causes bouts of insanity (though arsenic poisoning and bipolar disorder have also been suggested as possible causes).
George III routinely checked out from his royal duties to escape to seclusion and private recovery at Kew Palace. He was prone to babbling delusions in his later life and subjected to extreme treatments including strait-jackets, leeching, and ice baths to calm him. Modern medical testing shows porphyria was common in the highly inbred House of Hanover, to which King George III belonged.
George III spent the final decade of his reign in hiding and eventually lost his vision and hearing.