For My youngest Daughter Evey link matters KBG syndrome is a rare genetic disease that is the result of a mutation in the ANKRD11 gene at location 16q24.3. Only about a hundred known cases have been reported, although it is expected to be under-reported. The syndrome was first described by Herrmann in 1975 in three distinct families. Herrmann proposed the name KBG syndrome after the initials of affected families' last names, which aren't known to the general public.#kbg #kbgsyndrome #everylinkma
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For My youngest Daughter Evey link matters KBG syndrome is a rare genetic disease that is the result of a mutation in the ANKRD11 gene at location 16q24.3. Only about a hundred known cases have been reported, although it is expected to be under-reported. The syndrome was first described by Herrmann in 1975 in three distinct families. Herrmann proposed the name KBG syndrome after the initials of affected families' last names, which aren't known to the general public.#kbg #kbgsyndrome #everylinkma
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Short videos

0:15
For My youngest Daughter Evey link matters KBG syndrome is a rare genetic
27.3K viewsJun 13, 2023
TikTokamyelizabeth9191
0:19
KBG Syndrome Awareness: A Happy Baby's Journey
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TikToksengnky
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TikTokmrs.p.brandon
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TikTokkillerbeeguy
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¡La vuelta al cole y al insti ya es una realidad! 🎒✨
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YouTubeAsociacion Española Síndrome
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YouTubekbg content official.
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TikTokkhaferah
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