SITUS INVERSUS

Situs inversus (also called situs transversus) is a rare congenital condition in which the major visceral organs are reversed or mirrored from their normal positions. The normal arrangement is known as situs solitus. In other rare cases, in a condition known as situs ambiguus or heterotaxy, situs cannot be determined.
The term situs inversus is a short form of the Latin phrase "situs inversus viscerum," meaning "inverted position of the internal organs." Dextrocardia (the heart being located on the right side of the thorax) was first recognised by Marco Severino in 1643. However, situs inversus was first described more than a century later by Matthew Baillie.
The prevalence of situs inversus varies among different populations but is less than 1 in 10,000 people.[1]

Anatomy

Situs inversus causes the positions of the heart and lungs to be mirrored.
The condition affects all major structures within the thorax and abdomen. Generally, the organs are simply transposed through the sagittal plane.
The heart is located on the right side of the thorax, the stomach and spleen on the right side of the abdomen and the liver and gall bladder on the left side.
The left lung is trilobed and the right lung bilobed, and blood vessels, nerves, lymphatics and the intestines are also transposed.
If the heart is swapped to the right side of the thorax, it is known as situs inversus with dextrocardia or situs inversus totalis.
If the heart remains in the normal left side of the thorax, a much rarer condition (1 in 22,000 cases of situs inversus), it is known as situs inversus with levocardia or situs inversus incompletus.
Situs inversus with levocardia, or dextrocardia without situs inversus, present much higher rates of congenital defects than situs inversus with dextrocardia.

Significance

Situs inversus is generally an autosomal recessive genetic condition, although it can be X-linked or found in identical "mirror" twins.[2]
In the absence of congenital heart defects, individuals with situs inversus are phenotypically unimpaired, and can lead normal healthy lives, without any complications related to their medical condition.
There is a 5-10% prevalence of congenital heart disease in individuals with situs inversus totalis, most commonly transposition of the great vessels. The incidence of congenital heart disease is 95% in situs inversus with levocardia.
Many people with situs inversus are unaware of their unusual anatomy until they seek medical attention for an unrelated condition. The reversal of the organs may then lead to some confusion, as many signs and symptoms will be on the 'wrong' side.
For example, if an individual with situs inversus develops appendicitis, they will present to the physician with left lower abdominal pain, since that is where their appendix lies. Thus, in the event of a medical problem, the knowledge that the individual has situs inversus can expedite diagnosis. People with this rare condition should inform their physicians before an examination, so they may redirect their search for heart sounds and other signs.
Situs inversus also complicates organ transplantation operations as donor organs will almost certainly come from situs solitus donors. As hearts and livers are chiral, geometric problems arise placing an organ into a cavity shaped in the mirror image.
For example, a person with situs inversus who requires a heart transplant needs all the vessels to the transplant donor heart reattached to their existing ones. However, the orientation of these vessels in a person with situs inversus is reversed, necessitating steps so that the blood vessels join properly.

Kartagener syndrome

Situs inversus is generally inherited in an autosomal recessive pattern.
Further information: primary ciliary dyskinesia
About 25% of individuals with situs inversus have an underlying condition known as primary ciliary dyskinesia (PCD).
PCD is a dysfunction of the cilia that manifests itself during the embryologic phase of development.
Normally-functioning cilia determine the position of the internal organs during early embryological development, and so individuals with PCD have a 50% chance of developing situs inversus.
If they do, they are said to have Kartagener syndrome, characterized by the triad of situs inversus, chronic sinusitis, and bronchiectasis.
Cilia are also responsible for clearing mucus from the lung, and the dysfunction causes increased susceptibility to lung infections.
Male sufferers of PCD are often infertile: the cilia that make up the tail of individual sperm cells are also defective, thus rendering the sperm ineffective.