1 00:00:03,575 --> 00:00:06,555 Hey guys, Charlie from Top 10s here, and 2 00:00:06,555 --> 00:00:08,565 today, we're looking at ten kids you won't 3 00:00:08,565 --> 00:00:10,615 believe actually exist. 4 00:00:13,483 --> 00:00:16,563 In April of 2004, this baby was born in 5 00:00:16,563 --> 00:00:18,773 Peru, and caused a shock to her parents 6 00:00:18,773 --> 00:00:21,413 and hospital staff. She was born with an 7 00:00:21,413 --> 00:00:24,063 incredibly rare condition called sirenomelia. 8 00:00:24,063 --> 00:00:25,993 The condition causes the baby not to have 9 00:00:25,993 --> 00:00:28,153 any genitalia, meaning her gender wasn't 10 00:00:28,153 --> 00:00:30,553 verified for weeks. The disease also turns 11 00:00:30,553 --> 00:00:34,303 its victims into real-life mermaids. This 12 00:00:34,303 --> 00:00:36,103 is because the legs fuse together in the 13 00:00:36,103 --> 00:00:38,503 womb. Those with the condition have also 14 00:00:38,503 --> 00:00:40,973 been compared to snakes. The condition 15 00:00:40,973 --> 00:00:43,873 affects 1 in every 100 thousand babies born. 16 00:00:48,013 --> 00:00:50,253 Despite this not being funny whatsoever, 17 00:00:50,253 --> 00:00:52,523 7-year-old Connie Lloyd was born with a 18 00:00:52,523 --> 00:00:55,123 clown nose-shaped birthmark. A big red 19 00:00:55,123 --> 00:00:57,393 circular birthmark had been on her nose 20 00:00:57,393 --> 00:00:59,723 since she was born. Doctors said the rare 21 00:00:59,723 --> 00:01:01,933 condition could not be cured. However, 22 00:01:01,933 --> 00:01:04,003 after years of searching, the parents 23 00:01:04,003 --> 00:01:06,253 finally found a doctor able and willing to 24 00:01:06,253 --> 00:01:08,343 cure Connie. She was diagnosed with a 25 00:01:08,343 --> 00:01:10,503 (?) tumor and it was swiftly removed. 26 00:01:10,503 --> 00:01:12,973 Connie can now live a normal life without 27 00:01:12,973 --> 00:01:14,993 the encroaching birthmark. 28 00:01:19,309 --> 00:01:21,369 While Connie Lloyd had a nose that was too 29 00:01:21,369 --> 00:01:23,489 big, Tessa Evans was born with no nose at 30 00:01:23,489 --> 00:01:25,589 all. The now 2-year-old girl from Ireland 31 00:01:25,589 --> 00:01:27,799 has a smooth area where her nose should 32 00:01:27,799 --> 00:01:30,459 be. She has no sense of smell or sinuses. 33 00:01:30,459 --> 00:01:32,669 Despite having no nose, she can still 34 00:01:32,669 --> 00:01:36,089 cough, sneeze, and catch a cold. Tessa was 35 00:01:36,089 --> 00:01:38,429 lead to the first person to have cosmetic 36 00:01:38,429 --> 00:01:40,779 nasal surgery where a nose implant was 37 00:01:40,779 --> 00:01:43,499 fitted. Over years, the implant will 38 00:01:43,499 --> 00:01:45,599 encourage skin to grow over it, forming 39 00:01:45,599 --> 00:01:48,109 a real nose. The process will be done by 40 00:01:48,109 --> 00:01:50,129 the time she's a teenager. 41 00:01:53,426 --> 00:01:55,296 This 8-year-old boy was born with a large 42 00:01:55,296 --> 00:01:57,365 birthmark that covers half of his face. 43 00:01:57,365 --> 00:01:59,745 Since he has aged, the birthmark has grown 44 00:01:59,745 --> 00:02:01,905 further around his face, and grown thick 45 00:02:01,905 --> 00:02:04,115 black hair. A top Chinese plastic surgeon 46 00:02:04,115 --> 00:02:06,265 has agreed to treat him for free, due to 47 00:02:06,265 --> 00:02:09,005 the severity of his condition. The treatment 48 00:02:09,005 --> 00:02:11,145 will be in many stages, and will take up 49 00:02:11,145 --> 00:02:13,245 to 4 years. Despite this, I think it's 50 00:02:13,245 --> 00:02:15,435 worth it to remove the abnormally large 51 00:02:15,435 --> 00:02:16,915 hairy birthmark. 52 00:02:20,246 --> 00:02:22,296 This 4-year-old was born with a right 53 00:02:22,296 --> 00:02:24,596 foot that weighs nearly 1 stone. Verdeant 54 00:02:24,596 --> 00:02:26,636 is from India, and is still able to walk 55 00:02:26,636 --> 00:02:28,926 and run normally, despite his massive 56 00:02:28,926 --> 00:02:31,096 right foot. He's been bullied all his life 57 00:02:31,096 --> 00:02:33,546 and unable to attend school. Hundreds of 58 00:02:33,546 --> 00:02:35,756 doctors from India and other countries 59 00:02:35,756 --> 00:02:37,856 have examined his foot, but he is yet to 60 00:02:37,856 --> 00:02:40,346 be diagnosed. The only option doctors have 61 00:02:40,346 --> 00:02:42,686 suggested is to amputate the leg, however 62 00:02:42,686 --> 00:02:44,786 Verdeant's father is against this. 63 00:02:49,064 --> 00:02:51,474 This 8-year-old boy from Colombia was born 64 00:02:51,474 --> 00:02:53,444 with a turtle shell-like growth on his 65 00:02:53,444 --> 00:02:55,484 back. His village bullies him and they 66 00:02:55,484 --> 00:02:57,844 believe the dark forces caused the growth. 67 00:02:57,844 --> 00:03:00,234 He was also nicknamed "Turtle Boy" by the 68 00:03:00,234 --> 00:03:02,384 media, causing him to become incredibly 69 00:03:02,384 --> 00:03:04,654 depressed. A British doctor diagnosed 70 00:03:04,654 --> 00:03:06,804 Didier with an incredibly rare disease, 71 00:03:06,804 --> 00:03:09,014 saying it's the most extreme case he has 72 00:03:09,014 --> 00:03:11,464 ever seen. He's now in the UK getting free 73 00:03:11,464 --> 00:03:13,724 treatment for his life-altering condition. 74 00:03:17,572 --> 00:03:19,692 This 8-year-old Chinese boy was born with 75 00:03:19,692 --> 00:03:21,682 a fish scale-like skin disease. The 76 00:03:21,682 --> 00:03:23,892 disease is called (?) and he inherited it 77 00:03:23,892 --> 00:03:26,472 from his father. The disease is unfortunately 78 00:03:26,472 --> 00:03:29,352 incurable. The disease makes pants seem 79 00:03:29,352 --> 00:03:31,782 very thick, dry, itchy, and scaly. 1 in 80 00:03:31,782 --> 00:03:34,882 16 thousand babies are born with the disease per year. 81 00:03:34,882 --> 00:03:37,552 However, Pan has one of the most severe 82 00:03:37,552 --> 00:03:39,362 cases ever recorded. 83 00:03:43,875 --> 00:03:45,875 This 8-year-old Indian boy's giant 84 00:03:45,875 --> 00:03:47,955 deformed hands make his life a daily 85 00:03:47,955 --> 00:03:50,385 struggle. He doesn't attend school in case 86 00:03:50,385 --> 00:03:52,385 he scares the children or is bullied by 87 00:03:52,385 --> 00:03:54,805 them. He even struggles to eat because of 88 00:03:54,805 --> 00:03:57,175 his rare condition. His hand weighs about 89 00:03:57,175 --> 00:03:59,425 4 pounds, causing him to have a strong 90 00:03:59,425 --> 00:04:01,755 upper body. He'll be taken to a doctor in 91 00:04:01,755 --> 00:04:03,865 Delhi to have life-changing surgery on 92 00:04:03,865 --> 00:04:05,415 his hands soon. 93 00:04:08,433 --> 00:04:10,643 This 11-year-old Romanian gymnast is a 94 00:04:10,643 --> 00:04:12,943 child bodybuilder, and may be the world's 95 00:04:12,943 --> 00:04:15,193 strongest kid. He has worked out for 2 96 00:04:15,193 --> 00:04:17,473 hours a day since the age of 2. He rose 97 00:04:17,473 --> 00:04:19,863 to fame after his father posted a video of 98 00:04:19,863 --> 00:04:21,943 him performing a gymnastic stunt on 99 00:04:21,943 --> 00:04:24,233 YouTube. However, the father doesn't 100 00:04:24,233 --> 00:04:26,393 appreciate all of the attention, as child 101 00:04:26,393 --> 00:04:28,583 services are now looking into whether it's 102 00:04:28,583 --> 00:04:30,713 ethical to promote bodybuilding among 103 00:04:30,713 --> 00:04:32,113 children. 104 00:04:35,357 --> 00:04:37,487 This Chinese toddler was born with a dead 105 00:04:37,487 --> 00:04:40,037 unborn fetus of her twin inside her. Kang 106 00:04:40,037 --> 00:04:42,127 had already had a difficult start to life, 107 00:04:42,127 --> 00:04:44,307 as her parents abandoned her in a field, 108 00:04:44,307 --> 00:04:46,447 and she was forced to go into foster care. 109 00:04:46,447 --> 00:04:48,747 For some time, the toddler was practically 110 00:04:48,747 --> 00:04:51,207 pregnant with her dead twin sister. A year 111 00:04:51,207 --> 00:04:53,577 later, her carers had the fetus removed, as 112 00:04:53,577 --> 00:04:55,757 it was growing too big, and her neighbors 113 00:04:55,757 --> 00:04:58,077 had begun to call her a monster. Kang's 114 00:04:58,077 --> 00:05:00,047 incredibly rare condition only affects 115 00:05:00,047 --> 00:05:02,677 around 1 in 1.5 million births.