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- 23 de Mar, 2022
Speaking of rare genetic disorders we wish we could have lived without knowing
Allow me to introduce you to Roberts syndrome
[Ok so I can't embed photos from any device at my current location, unfortunately there will be no spoilers. You have been warned. I am very sorry.]
In the images, you see we have some glorious examples of cleft lip, cleft palate, bilateral cleft lip, phocomelia (shortened limbs). Oh, and that weird drawing? That's an 18th century study of a stillborn with Roberts syndrome.
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Wow I really wish I didn’t know about holocephaly. I’d seen cyclops babies before but didn’t know the name for it.
The eyes on the middle one will probably chase me in a nightmare tonight.
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Allow me to introduce you to Roberts syndrome
[Ok so I can't embed photos from any device at my current location, unfortunately there will be no spoilers. You have been warned. I am very sorry.]
Roberts Syndrome (aka pseudothalidomide syndrome or tetraphocomelia) is a disorder caused by a mutation in the ESCO2 gene on chromosome 8. It disrupts cell growth and division, specifically by causing "puffing" in the centromeres, or the glue that holds chromosomes together. This causes arms and legs to be shortened, facial deformities, bone loss, etc. Autosomal recessive. So rare the condition is not known, but a few years ago I read that there were supposedly 250 known cases of Roberts syndrome in the world.
In the images, you see we have some glorious examples of cleft lip, cleft palate, bilateral cleft lip, phocomelia (shortened limbs). Oh, and that weird drawing? That's an 18th century study of a stillborn with Roberts syndrome.
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