TikToker’s Miracle Survival Story #shorts #tiktokinfluencer #fontaineprogeroidsyndrome
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YouTubePinkNews
TikToker’s Miracle Survival Story #shorts #tiktokinfluencer #fontaineprogeroidsyndrome
TikToker’s Miracle Survival Story #shorts #tiktokinfluencer #fontaineprogeroidsyndrome Meet Kenzie, a 26-year-old influencer and one of just 13 people in the world living with Fontaine progeroid syndrome. With over 680,000 followers on TikTok, she shares get-ready-with-me videos, cooking content, and moments from her daily life — all while ...
31.2K views2 weeks ago
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Fontaine Progeroid Syndrome
2:59
Fontaine Progeroid Syndrome
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1.2K views1 month ago
As of December 2025, this is where the 156 children and young adults with Hutchinson-Gilford Progeria Syndrome (HGPS) live, all with a progerin-producing mutation in the LMNA gene; and 83 people in the category of progeroid laminopathy (PL), who have mutations in the lamin pathway but do not produce progerin; in a total of 51 countries. Want to learn more? Visit our Find the Children website page: https://www.progeriaresearch.org/find-the-children/ 💙 Help The Progeria Research Foundation (PRF)
0:31
As of December 2025, this is where the 156 children and young adults with Hutchinson-Gilford Progeria Syndrome (HGPS) live, all with a progerin-producing mutation in the LMNA gene; and 83 people in the category of progeroid laminopathy (PL), who have mutations in the lamin pathway but do not produce progerin; in a total of 51 countries. Want to learn more? Visit our Find the Children website page: https://www.progeriaresearch.org/find-the-children/ 💙 Help The Progeria Research Foundation (PRF)
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GEEZ TV on Instagram: "Meet the family in Nigeria living with a incredibly rare condition called Cutis Laxa. While these children are only 6 and 8 years old, the condition causes their skin to wrinkle, giving them the appearance of elders. Medical experts have identified this as a progeroid condition—a 1-in-a-million genetic occurrence. These kids are proving that beauty and strength come in all forms, and they aren't letting anyone's comments stop them from living their best lives which is all
1:37
GEEZ TV on Instagram: "Meet the family in Nigeria living with a incredibly rare condition called Cutis Laxa. While these children are only 6 and 8 years old, the condition causes their skin to wrinkle, giving them the appearance of elders. Medical experts have identified this as a progeroid condition—a 1-in-a-million genetic occurrence. These kids are proving that beauty and strength come in all forms, and they aren't letting anyone's comments stop them from living their best lives which is all
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Fontaine Progeroid Syndrome
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YouTubeMackenzie Gomez
As of December 2025, this is where the 156 children and young adults with Hutchinson-Gilford Progeria Syndrome (HGPS) live, all with a progerin-producing mutation in the LMNA gene; and 83 people in the category of progeroid laminopathy (PL), who have mutations in the lamin pathway but do not produce progerin; in a total of 51 countries. Want to learn more? Visit our Find the Children website page: https://www.progeriaresearch.org/find-the-children/ 💙 Help The Progeria Research Foundation (PRF)
0:31
As of December 2025, this is where the 156 children and young adults …
96 views2 weeks ago
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GEEZ TV on Instagram: "Meet the family in Nigeria living with a incredibly rare condition called Cutis Laxa. While these children are only 6 and 8 years old, the condition causes their skin to wrinkle, giving them the appearance of elders. Medical experts have identified this as a progeroid condition—a 1-in-a-million genetic occurrence. These kids are proving that beauty and strength come in all forms, and they aren't letting anyone's comments stop them from living their best lives which is all
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