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What else can I help you with?
What is the worst eye disease in children?
xerophthalmia
How do you find the greatest common factor when there are no common factors?
There is always a common factor. If there are no common prime factors, the GCF is 1.
A is a common multiple of two or more denominators?
It is possible that A has such properties.
What is the least common multiple of two ir more denominators?
That's the least common denominator or LCD.
How common is?
it is not very common zirconium is found on excess gold so it is pretty common
What is the worst eye disease in children?
xerophthalmia
What can a dietary deficiency of vitamin A produce?
xerophthalmia
What lack of nutrient is caused by xerophthalmia?
Vitamin A
Drying of the cornea due to vitamin A deficiency is called?
xerophthalmia
Is Xerophthalmia characterized by the loss of luster of the conjunctiva and cornea?
True
Deficiency of which vitamin caused xerophthalmia?
deficiency of vitamin A causes xerophthalmia but there can be other causes also. In this defect eye fails to produce tears because of dryness off cornea
Deficiency of Vitamin A causes?
defiency of vitamin a causes blindness.
What do you get from lack of vitamin a?
Night blindness, measles, slow bone development, Xerophthalmia
Who discovered xerophthalmia?
Oomen in 1961 , Mc laren in 1963 and ten doesschate in 1969
What is xerophthalmia?
Xerophthalmia is a medical condition characterized by dry eyes due to a lack of adequate tear production. It is commonly caused by vitamin A deficiency and can lead to serious eye problems if left untreated, such as corneal damage and vision loss. Treatment typically involves addressing the underlying nutrient deficiency and using lubricating eye drops.
What is xeropthalmia?
Xerophthalmia is the medical term for "dry eye", a condition which is caused by decreased tear production.
Deficiency of which of the following causes xerophthalmia?
Hello, I see you are asking "What are the causes for cps deficiency?" CPS1 deficiency is caused by alterations in the CPS1 gene and is inherited in an autosomal recessive pattern. Diagnosis is based on symptoms, laboratory testing, and genetic testing. You can also visit this site - digestive tract health. com/condition/cps-deficiency/c/7434
