Although each person is born with a unique set of genes, when kids are born, it’s impossible to avoid conversations about who they look the most like. And some people are lucky enough to find resemblances to their older ancestors, like a bolt from the blue. With children looking like an exact copy of their parents and grandparents, we’re almost ready to believe that it’s a result of some kind of reincarnation or wizardry.
And while scientists are still scratching their heads about our genes, we at Bright Side simply can’t help but wonder about what miracles nature is really capable of.
1. Princess Diana and her grandmother, Cynthia, made us wonder whether time travel already exists.
2. “A side by side of my 3x great-grandmother and my mother”
3. “I think I might be a clone and no one told me.”
4. This family’s genes are so strong.
5. “My dad and me, 1980 vs 2020”
6. “This is me in the mid-’90s and my son in 2020, not quite the same pose, but I like seeing the similarities!”
7. “My grandmother (1940) and me (2005) — I feel grateful to carry on her lovely genes.”
8. “I think it’s fun to look at my dad at 12 vs me at 12.”
9. “Me vs my mom’s yearbook photo (1977)”
10. “My son at a year old in 2004 and his great-great-grandfather at the same age in 1882”
11. “My whole life people have told me I look just like my mom when she was my age. I never saw it until I found this old picture of my mom.”
12. Nature’s miracles with genes will never cease to amaze us.
13. “My dad and me, both at the age of 14”
14. “Found this old picture of my great-grandma. I was amazed at how much I look like her!”
15. This mom and daughter look almost identical.
16. Seems like sometimes nature works like a 3D printer.
17. This granddaughter has features similar to her grandmother, and they both look so beautiful.
18. “My ancestor from the 1700s next to my dad — apparently my family’s looks haven’t changed much.”
19. “My dad’s mother and me, 70 years apart”
20. This bright smile passed through at least 2 generations.
Bonus: Princess Charlotte and Queen Elizabeth might not look alike, but the princess is surely the queen’s mini-me.
Have you seen this kind of resemblance in real life? Do you know any relatives that look like you?
Preview photo credit JUSTIN TALLIS /AFP / Getty Images, Max Mumby/Indigo / Getty Images Entertainment / Getty Images
Meet Twins with the Rare Benjamin Button Syndrome, Who Became Symbols of Resilience
In a small Brazilian town, there resides an extraordinary duo of identical twins named Elis and Eloá. Their story serves as a beacon of resilience and the remarkable power of the human spirit. Afflicted with Hutchinson-Gilford Progeria Syndrome, a rare and fatal genetic disorder causing accelerated aging, these twins confront their adversities with remarkable grace and strength, earning admiration from people worldwide.
Understanding Hutchinson-Gilford Progeria syndrome
HGPS stands as an exceptionally rare disorder, impacting roughly 1 in 20 million newborns globally. Marked by rapid aging from early childhood, individuals with progeria often display growth delays, diminished body fat and hair, prematurely aged skin, joint stiffness, and severe cardiovascular issues. Typically, those with HGPS have an average life expectancy of about 14.5 years, though some may extend into their late teens or early twenties. This syndrome gained public attention through the film The Curious Case of Benjamin Button.
The condition is caused by a mutation in the LMNA gene, which produces the lamin A protein responsible for maintaining the structural integrity of the cell nucleus. The mutation results in the production of an abnormal version of the protein, called progerin, which causes cells to become unstable and die prematurely.
Elis and Eloá’s journey
Elis and Eloá swiftly captured attention because of their distinctive medical condition. Despite the physical hurdles imposed by progeria, their contagious smiles and steadfast optimism have emerged as beacons of hope and inspiration. Guilherme and Elismar, the twins’ parents, have dedicated their lives to offering the utmost care for their daughters, striving to ensure they experience as normal a life as feasible within the confines of their condition.
The family’s path has been far from easy. Their daily life is filled with demanding medical routines, including physiotherapy, aimed at addressing joint stiffness and preserving mobility. Despite these challenges, Elis and Eloá approach each day with remarkable bravery and an unparalleled enthusiasm for life, which is truly remarkable.
A global community of support
Elis and Eloá’s narrative has touched hearts worldwide, sparking a surge of solidarity from individuals and groups committed to promoting awareness about progeria and backing research endeavors. The Progeria Research Foundation, a pivotal entity in this realm, has played a vital role in propelling research forward and furnishing assistance to families grappling with the condition.
Through social media platforms, the twins’ journey is shared with a broad audience, fostering a sense of community and solidarity. Their family’s updates, documenting both the highs and lows of their daily lives, provide invaluable insights into the realities of living with progeria, while also spreading a message of hope and perseverance.
Advances in research and hope for the future
In recent years, there have been remarkable advancements in comprehending and addressing progeria. A notable milestone occurred in 2020 when the U.S. Food and Drug Administration (FDA) granted approval for the first progeria treatment: lonafarnib. This medication has demonstrated efficacy in prolonging the lives of children with progeria by mitigating the accumulation of progerin in cells, thereby decelerating the disease’s advancement.
Though a cure remains elusive, ongoing research presents promising prospects. Scientists are delving into gene-editing methodologies, like CRISPR, as potential means to rectify the genetic mutation at its root. For families such as Elis and Eloá’s, these breakthroughs offer a ray of hope for the future.
And in our other article, we recounted the remarkable story of a girl born without a nose, affectionately dubbed “Voldemort,” who refuses to let her differences define her.
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