Triple X Syndrome‚ also known as XXX Syndrome‚ is a genetic disorder affecting the sex chromosomes. Females generally posses two X chromosomes‚ one from each parents‚ but females affected by Triple X syndrome possess three X chromosomes. On average‚ Triple X Syndrome affects 1 in 1000 females. Triple X syndrome generally doesn’t occur due to inheritance‚ but is rather caused by an error in the formation of the gametes known as nondisjunction‚ resulting in the extra X chromosome. Another cause of Triple
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Shwachman Diamond Syndrome (SDS) is an inherited condition that affects mainly the bone marrow‚ pancreas‚ and skeletal system of the human body. Bone marrow produces new blood cells; however‚ in a patient with SDS‚ the bone marrow does not make all of the types of white blood cells making the body more vulnerable to infection. The pancreas produces enzymes that help break down and use nutrients from food. SDS results in the pancreas not producing enough of these enzymes‚ which makes it hard to digest
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Increased Mortality among Widowers by Parkes‚ Benjamin‚ and Fitzgerald was published in the British Medical Journal in 1969. The authors goal was to determine if there was any validity to the “broken heart syndrome” and to discover what the actual mortality rate in connection with the “broken heart syndrome”. The population of this study included widowers 55 years of age and older and the sample used was 4‚486 widowers 55 years of age and older. The study was completely observation as the men were followed
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Treacher Collins Syndrome is believed to be caused by a change in the gene on chromosome 5‚ which affects facial development. About 40 percent of the time‚ one parent has the Treacher Collins Syndrome gene. Geneticists can now determine whether the Treacher Collins gene is a new mutation or one that has been passed on. There are new studies being done to see about the possibilities of there being other genes that could be involved with this syndrome. Treacher Collins Syndrome is believed to be
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Alien Hand Syndrome This is a proposed neurological disorder that is characterized by the affected person’s own hand or hands that seemingly have taken over its own free will or mind of its own.. It happens when someone your hand moves alone. they are not in control of it as if it isn’t part of the body. It is believed that it is a result from a brain surgical intervention‚ in treatment of worst cases of epilepsy. Some reports would also say that this condition can be acquired after a cerebrovascular
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For this criterion I will discuss the current and also the future patterns in the UK.I will also discuss who is going to be affected by the new changes and will provide statistics to support my answer which is also going to discuss the inequalities of health. There are many factors which affect the health of the public who are in the United Kingdom. However the UK has become a better place to live in compared to living here in the 19 or 2oth century. The main disadvantage is always due to social
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complications to occur. While many of the potential side effects and complications that can arise with medications are minor or uncommon‚ there are others that can be very serious and have potential for mortality. Stevens Johnson Syndrome (SJS) and Toxic Epidermal Necrolysis Syndrome (TENS)‚ are both a form of a very serious and rare skin disorder‚ that could result in death‚ due to adverse drug reactions. This disease affects the skin and mucous membranes‚ in which the layers of the skin start
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The common cause of congenital myasthenic syndromes is genetics‚ affecting the junction where the nerve triggers muscle activity. The inherited autosomal recessive gene exists in both parents‚ who pass the mutated gene to the offspring. The syndrome appears shortly after birth or early childhood. Severity ranges from minor to increasing concentrations of muscle weakness. There are over twenty different genes known to cause congenital myasthenic syndromes‚ as different as each individual. Sometimes
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Super Duper® Handy Handouts!™ Number 116 What is Down Syndrome? by Becky L. Spivey‚ M.Ed. What is Down syndrome? Down syndrome is a congenital disorder stemming from a chromosomal abnormality appearing in one of every 800 births. It is the most common genetic disorder affecting more than 5‚000 babies born in the United States each year. This syndrome occurs when one chromosome has an extra “part‚” an error occurs in cell division‚ or an extra chromosome exists resulting in 47 chromosomes. Most
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Turner Syndrome Intro Turner Syndrome is a genetic disorder involving a chromosomal defect in females. Turner Syndrome occurs when a woman is missing part or all of an X-chromosome. Though this disease has a wide range of side effects‚ the most common are physical characteristics such as short height and incomplete development. It all depends on how many of the body’s cells are affected by the changes to the X chromosome. This disease affects one in every 2‚500 - 3‚000 girls‚ with 800 affected
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