Many people are unaware of the symptoms of primary dwarfism caused by microcephalic osteodysplastic type II. In short, it is a complex kind of dwarfism in which there is no more bodily growth. There isn’t another option in this circumstance.
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It was unfortunate that Abigail Lee was born with this type of genetic condition.
The image appears typical at first glance: a child is seated in a stroller, however in this instance, the stroller is a dollhouse toy.
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Even though Abigail is two years old, her weight of nine pounds is comparable to that of a newborn.
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The young girl’s estimated growth size, according to the doctors, is 23 inches. The child’s health is excellent. She develops, eats, and plays, yet she doesn’t gain weight.
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Though there is now no known treatment for this kind of dwarfism, scientific advancements in the future are still hoped to be beneficial.
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It is Abigail’s right to go to school and lead a long, happy life. Our wish is that she would experience happiness and self-satisfaction.
Source: https://lifeblogs.am/2023/10/31/destined-to-always-be-doll-size-a-look-at-little-thumbelina-girls-life-in-the-present/