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Poland syndrome: definition, symptoms and risk factors

Definition

Poland syndrome is a disorder in which affected individuals are born with missing or underdeveloped muscles on one side of the body, resulting in abnormalities that can affect the chest, shoulder, arm, and hand. The extent and severity of the abnormalities vary among affected individuals.

 

History

It was first named in 1962 by Patrick Clarkson, a New Zealand-born British plastic surgeon working at Guy’s Hospital and Queen Mary’s Hospital, London. He noticed that three of his patients had both a hand deformity and an underdeveloped breast on the same side. He discussed this with his colleague at Guy’s Hospital, Dr Philip Evans, who agreed that the syndrome was “not widely appreciated”. Clarkson found a reference to a similar deformity published by Alfred Poland, over a hundred years earlier in Guy’s Hospital reports, in 1841. Clarkson was able to find the hand specimen dissected by Poland, which was still held in the hospital pathology museum.

Poland had dissected a convict known as George Elt, who was said to be unable to draw his hand across his chest. Poland noted the chest wall deformity, and this was illustrated in his article; the hand was also dissected and preserved for posterity in Guy’s Hospital museum where it remains today. It cannot be truly said that Poland described this syndrome because he only described one isolated case. Clarkson published his series of three cases and named the syndrome after Poland in his article.

Epidemiology

According to the National Human Genome Research Institute, Poland syndrome affects males three times as often as females and affects the right side of the body twice as often as the left. The incidence is estimated to range from one in 7,000 to one in 100,000 live births. The incidences of the affected males are twice as much as that of females. In cases when the severity is mild, the condition is not diagnosed until puberty. Due to the same reasons the condition is often underreported and misdiagnosed.

Risk factors

Currently no risk factors have been identified for Poland Syndrome.

It is important to note that having a risk factor does not mean that one will get the condition. A risk factor increases ones chances of getting a condition compared to an individual without the risk factors. Some risk factors are more important than others.

Also, not having a risk factor does not mean that an individual will not get the condition. It is always important to discuss the effect of risk factors with your healthcare provider.

Causes

The exact cause of Poland syndrome is not known. However, researchers think that the syndrome develops in a fetus around the six-week mark. At this stage of gestation, the fetus is dependent on blood flow for development. Poland syndrome could present itself when there is an interruption in blood flow to tissues around the chest and ribcage.

Researchers aren’t sure whether or not someone can inherit Poland syndrome. There aren’t any clear genetic markers for the condition. It’s possible but rare to have more than one person in the same family with the condition. Even then, each person usually has varying levels of severity.

Symptoms of poland syndrome

People who have Poland syndrome have an asymmetrical body frame. Their chest muscle lacks development on one side of their body, which can create a seemingly lopsided position. All signs of Poland syndrome occur on one single side of the body only.

Signs of the condition may include:

Complications of poland syndrome

Diagnosis and tests

The diagnosis of Poland Syndrome is usually made at birth based upon characteristic physical findings, a thorough clinical evaluation, and a variety of specialized tests. Such tests may include advanced imaging techniques, such as a CT scan that can determine the extent to which the muscles may be affected. During CT scanning, a computer and X-rays are used to create a film showing cross-sectional images particular organs or structures within the body. X-ray studies may be used to help identify and characterize specific abnormalities in the hands, forearms, ribs, and/or shoulder blades.

Treatment and medications

Prevention of poland syndrome

Currently there are no definitive methods available to prevent Poland Syndrome. A majority of cases are sporadic and hence, no preventive measures are available. A few cases have been reported as being inherited as an autosomal dominant trait. Hence, for such cases:

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