Abstract
The role of genetic mutations on genes PAX2 & PAX6 in cyclopia syndrome
Highlights
Cyclopia syndrome is a rare disorder of holoprosencephaly that occurs with birth defects
Cyclopia syndrome is a rare genetic disorder that has been reported in only a few cases in the medical world, and most are preserved at the vrolik Amsterdam Museum of Medicine in the Netherlands (Figure 2) [1]
In 2006, a baby girl in India was born with cyclopia syndrome who died a day after giving birth
Summary
Cyclopia syndrome is a rare disorder of holoprosencephaly (fracture of the brain in the fetus) that occurs with birth defects. In this disease, the orbit of the eye is divided into two very close caverns, with either the monocular organism being seen or the binoculars being closely related. The orbit of the eye is divided into two very close caverns, with either the monocular organism being seen or the binoculars being closely related The syndrome affects both animals and humans, with the frequency in animals 1 in every 16,000 births and in the human fetus 1 in 250 births (Figure 1) [1]
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