Answer:
A which is coal ok tell me if I am right
Answer:
Explanation:
Galactosemia is an inherited metabolic disorder caused by changes, or mutations, in both copies of an individual’s GALT gene. In the majority of cases, children with galactosemia do not have parents with galactosemia. Mother and father separately are a silent carrier of the condition, which is expressed in the child (autosomal recessive inheritance).
Each individual has two copies of the GALT gene – one from father and one from mother. In case of any changes of these genes (mutations) that prevents the gene from working correctly. In order to inherit galactosemia, it is necessary for a child to have two GALT gene changes. In case of one GALT gene change there is no galactosemia.
Infants with galactosemia may be identified through newborn screening programs or by symptoms that present during the first few weeks of life. Untreated infants develop liver and kidney disease, cataracts in their eyes, and serious infections.
Bones: they lose calcium, becoming crispy
Muscle: they lose mass
Cartilage: becomes stiffer, but it does not make airway more rigid
D) connective tissue: It includes bone, blood, and lymph tissue, giving support to the skin and internal organs, becoming increasingly stiff when aging.
It should be connective tissue.
The answer is Filarial parasites. They belong to the group of roundworms of the Filarioidea type. An example of a filarial worm is the Wuchereria bancrofti. These organisms cause lympathic filariasis (LF) which is characterized by edema. They are spread by the mosquito vector.
