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Cyclopia (named after the Greek mythology characters cyclopes), also known as alobar holoprosencephaly, is the most extreme form of holoprosencephaly and is a congenital disorder (birth defect) characterized by the failure of the embryonic prosencephalon to properly divide the orbits of the eye into two cavities.
The baby only has one eye because his eye sockets did not form correctly in the womb. Doctors believe that the birth defect could be resultant of a combination of medicines that the mother took.
Waardenburg syndrome is a group of rare genetic conditions characterised by at least some degree of congenital hearing loss and pigmentation deficiencies, which can include bright blue eyes (or one blue eye and one brown eye), a white forelock or patches of light skin.
Congenital blindness is a hereditary disease and can be treated by gene therapy. Visual loss in children or infants can occur either at the prenatal stage (during the time of conception or intrauterine period) or postnatal stage (immediately after birth). [3] There are multiple possible causes of congenital blindness.
The colored part of the eye is. Many babies are born with blue eyes, and then their eyes change color as their genes continue to develop. ... All blue-eyed people can trace their ancestry back to ...
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Leber congenital amaurosis (LCA) is a rare inherited eye disease that appears at birth or in the first few months of life. [2]It affects about 1 in 40,000 newborns. [1] LCA was first described by Theodor Leber in the 19th century.
From birth, the pupils of an infant remain constricted to limit the amount of entering light. In regards to pupil dimensions, newborns' pupils grow from approximately 2.2 mm to an adult length of 3.3 mm. [2] A one-month-old infant can detect a light threshold only when it is approximately 50 times greater than that of an adult. By two months ...