Thursday, March 30, 2017

SICLE CELL DISEASE (SICLE CELL ANAEMIA)



Sickle cell disease is a group of disorders that affects hemoglobin, the molecule in red blood cells that delivers oxygen to cells throughout the body. People with this disorder have atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape.



The term sickle cell disease (SCD) describes a group of inherited red blood cell disorders. People with SCD have abnormal hemoglobin, called hemoglobin S or sickle hemoglobin, in their red blood cells.
Hemoglobin is a protein in red blood cells that carries oxygen throughout the body.
“Inherited” means that the disease is passed by genes from parents to their children. SCD is not contagious. A person cannot catch it, like a cold or infection, from someone else.
People who have SCD inherit two abnormal hemoglobin genes, one from each parent. In all forms of SCD, at least one of the two abnormal genes causes a person’s body to make hemoglobin S. When a person has two hemoglobin S genes, Hemoglobin SS, the disease is called sickle cell anemia. This is the most common and often most severe kind of SCD.
Hemoglobin SC disease and hemoglobin Sβ thalassemia (thal-uh-SEE-me-uh) are two other common forms of SCD.

Some Forms of Sickle Cell Disease

  • Hemoglobin SS
  • Hemoglobin SC
  • Hemoglobin Sβthalassemia
  • Hemoglobin Sβ+ thalassemia
  • Hemoglobin SD
  • Hemoglobin SE

Overview

Cells in tissues need a steady supply of oxygen to work well. Normally, hemoglobin in red blood cells takes up oxygen in the lungs and carries it to all the tissues of the body.
Red blood cells that contain normal hemoglobin are disc shaped (like a doughnut without a hole). This shape allows the cells to be flexible so that they can move through large and small blood vessels to deliver oxygen.
Sickle hemoglobin is not like normal hemoglobin. It can form stiff rods within the red cell, changing it into a crescent, or sickle shape.
Sickle-shaped cells are not flexible and can stick to vessel walls, causing a blockage that slows or stops the flow of blood. When this happens, oxygen can’t reach nearby tissues.




Friday, March 3, 2017

HUMAN JOINT.

Joint: This is the point at which two or more bones meet.

This video explains different kinds and types of joints, I hope you enjoy it.


THE SKELETAL SYSTEM OF HUMAN!

The human skeleton is the internal framework of the body.

It is composed of around 300 bones at birth – this total decreases to 206 bones by adulthood after some bones have fused together.

The bone mass in the skeleton reaches maximum density around age 20.

 The human skeleton can be divided into the axial skeleton and the appendicular skeleton.

The axial skeleton is formed by the vertebral column, the rib cage, the skull and other associated bones.

The appendicular skeleton, which is attached to the axial skeleton, is formed by the shoulder girdle, the pelvic girdle and the bones of the upper and lower limbs.
The human skeleton performs six major functions;

1:Support,
2: Movement,
3:Protection,
4:Production of blood cells,
5:Storage of minerals,
6:Endocrine regulation.
The human skeleton is not as sexually dimorphic as that of many other primate species, but subtle differences between sexes in the morphology of the skull,dentitionlong bones, and pelvis exist.

 In general, female skeletal elements tend to be smaller and less robust than corresponding male elements within a given population. The human female pelvis is also different from that of males in order to facilitate child birth.
Unlike most primates, human males do not havepenile bones.

DivisionsEdit



Axial skeletonEdit

Main article: Axial skeleton
The axial skeleton (80 bones) is formed by the vertebral column (32–34 bones; the number of the vertebrae differs from human to human as the lower 2 parts, sacral and coccygeal bone may vary in length), a part of the rib cage (12 pairs ofribs and the sternum), and the skull (22 bones and 7 associated bones).
The upright posture of humans is maintained by the axial skeleton, which transmits the weight from the head, the trunk, and the upper extremities down to the lower extremities at the hip joints. The bones of the spine are supported by many ligaments. The erector spinae muscles are also supporting and are useful for balance.


Appendicular skeletonEdit

Main article: Appendicular skeleton
The appendicular skeleton (126 bones) is formed by the pectoral girdles, the upper limbs, the pelvic girdle or pelvis, and the lower limbs. Their functions are to make locomotion possible and to protect the major organs of digestion, excretion and reproduction.