Answer:
The correct answer is d.
Explanation:
Hydranencephaly is a rare congenital anomaly characterized by the absence and replacement of the cerebral hemispheres by cerebrospinal fluid and necrotic remains, with preservation of the membranes (leptomeninges), within a skull of normal capacity and shape. It is the most severe form of cortical destruction cerebral bilateral and is considered an extreme form of porencephaly (focal cystic cavity). It mainly affects the territory of the internal carotid artery and middle cerebral artery, with preservation of the territories supplied by the vertebrobasilar arteries. The most accepted etiology is carotid vascular insufficiency, due to multiple causes (bleeding, placental thromboembolism, arteritis, vascular malformations, among others).
Mass is the amount of matter in any object.
Answer:
b. Even though the DNA sequence changed, the sequence still codes for the same amino acid, so no change in phenotype will occur.
Explanation:
There is redundancy in the genetic code. That means that different codons can code for the same amino acids, so some mutations do not change the amino acid sequence of the protein.
Here, the amino acid is unchanged with the mutation.
If the amino acid sequence of the protein is the same, then the protein is not changed, so there will be no change in the phenotype
