What is pericardium membrane, and pericardium fluid ?​

Your heart is surrounded by a double-layered membrane, called the pericardium or pericardial sac. ... There is a very small amount of fluid called pericardial fluid in the pericardial sac. This fluid helps to decrease friction between the pericardial layers. It also allows for smooth movement of the heart when it beats

Explanation:

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PERICARDIUM MEMBRANE

The pericardium acts as mechanical protection for the heart and big vessels, and a lubrication to reduce friction between the heart and the surrounding structures. A very important role in all aspects of pericardial functions is played by mesothelial cells.

Our heart is surrounded by a double-layered membrane, called the pericardium or pericardial sac. This membrane keeps your heart in place in your chest cavity, restricts the expansion of your heart when your blood volume increases, and helps to protect your heart.

PERICARDIUM FLUID

Pericardial fluid is the serous fluid secreted by the serous layer of the pericardium into the pericardial cavity. ... This serous layer has two membranes which enclose the pericardial cavity into which is secreted the pericardial fluid.

an individual’s sex (i.e., whether they are a male or female) is determined by the sex chromosomes. most people have two sex chromosomes, one that is inherited from their mother and one that is inherited from their father. typically, females have two x chromosomes (xx) and males have one x chromosome and one y chromosome (xy). conditions caused by changes (“mutations”) in genes located on the x chromosome are considered x-linked.

x-linked recessive inheritance

most x-linked conditions are recessive. this means that in a person with two x chromosomes (most females), both copies of a gene (i.e., one on each x chromosome) must have a change or mutation whereas in a person with one x chromosome (most males), only one copy of a gene must have a mutation. a female with a mutation in one copy of a gene on the x chromosome is said to be a “carrier” for an x-linked condition. a male with a mutation in a gene on the x chromosome is typically affected with the condition. because females have two copies of the x chromosome and males have only one x chromosome, x-linked recessive diseases are more common among males than females. however, x-linked recessive diseases can occur in both males and females.

for x-linked recessive disorders, an unaffected carrier mother who has a mutation in a gene on the x chromosome can transmit either the x chromosome with this mutation or a “normal” x chromosome to her children. if the father is unaffected, none of her daughters will be affected and all of her daughters will be unaffected—since they will inherit at least one normal x chromosome from their father. however, each daughter will have a 50% chance of being an unaffected carrier like her mother and a 50% chance of both x chromosomes being normal.

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