Answer:
If a female child has hemophilia it is possible that the mother is a carrier of the hemophilia gene and the father has hemophilia.
Explanation:
- A daughter gets X chromosome from both her parents.
- It is generally seen in males.
- Hemophilia is generally recessive in females.They act as carriers of hemophilia. This occurs because they have a X chromosome that dominates the hemophilia affected gene that they inherit from any parent.
- But, if both the parents have faulty genes ,i.e the mother is the carrier of the gene and the father is hemophiliac, then the chances are the daughter has hemophilia too.
Answer:
Cells from the cheek are a type of epithelial cell, similar to skin. ... They can be seen faintly even at 40x (scanning power), but the most dramatic images are at 400x where the nucleus is clearly visible as a dark spot in the center of the cell.
Explanation:
pancreas
Explanation:
In addition to the GI tract, there are digestion accessory organs (salivary glands, pancreas, gallbladder, and liver) that play an integral role in digestion. The accessory organs do not come directly in contact with food or digestive content.
Answer: Rheumatoid arthritis
Explanation:
Rheumatoid arthritis is a disease which is a autoimmune disease which is usually associated with the pain and inflammation in the joints. This is the condition in which the person is not able to walk or sit for a longer period of time as it is painful.
The lysosomes is an enzyme that is found in the saliva and tears of human beings which helps in the degradation of the cell wall.
In case of autoimmune diseases the antibody present in the body destroys the cells of the body considering it as self antigen. Its concentration is found high in the people suffering from this autoimmune disorder.
