Malanie Gaydos Genetic Disorder

Melanie Gaydos from New York , U.S.A has a genetic condition called ectodermal dysplasia.Ectodermal dysplasia makes skin extremely sensitive, teeth weak, and hair grow inward.Her condition occurred when she first started the transformation process of changing into the specialized cells that form all parts of the body . When the cells in her surface layer should’ve become specialized , something had gone wrong. The cells that make up her skin.hair, teeth , and nails didn’t take on all the vital properties that make those parts of her body work. What I admire most from Melanie is that despite everything she’s gone through; she came through in the end as an international model.

Furthermore, people born with this unique genetic defect share some similar characteristic traits and features that are both physical

The purpose of this paper is to discuss the effects of the disorder and how genetics and biochemistry work together to create this

In situs inversus the visceral organs are reversed as well as the heart. Most of the time dextrocardia with situs inversus patients do not have any health problems that have to do with the condition and can live a normal and healthy life. The most common issue with isolated dextrocardia is decreased number of cilia which results in a weaker immune system. In the case of situs solitus the heart is either just in the right thoracic region or a mirror image and the other visceral organs are in their normal place; this anatomical confliction results in health issues and heart deformities. Situs solitus causes bigger problems more often and affects mainly the respiratory,digestive,endocrine and hepatic systems. It can cause health issues ranging from abdominal obstructions to deformities,asplenia and liver problems that result in jaundice. In many cases cardiopulmonary deformities result in respiratory problems usually leading to lack of oxygen and hindered development and growth. Although dextrocardia is a congenital condition and has unknown causes , there are factors that contribute to the chances of development of the condition in utero. Sometimes dextrocardia is a result of the heart developing as a mirror image and as a result of that migrating to the right side of the chest. Another common reason dextrocardia develops is that through defects in the thoracic and abdominal area

grow more and more complex. In a topic that has been debated for over a decade, embryonic

Randy Foyer suffers from a different genetic disorder. His organs are mirrored. For example, his heart is on his right side instead of his left. About 19 days in pregnancy, a structure called cilia is supposed to spin, turning all his genes on the

complex disease since it affects various parts of the body. The gene mutation causes a defect of a

The exact cause of this condition is not known. The condition may be passed down through families through an abnormal gene.

I was born with a birth defect known as Ectodermal dysplasia. Ectodermal dysplasia has over 150 classified types that all have their own effects

According to the Centers for Disease Control and Prevention there are approximately three million babies born in the United States each year (Martin et al.). While there is always risk that a baby could have any number of health conditions, one rarely occurring condition is situs inversus. “Situs” refers to the position of an organ, with situs solitus being the ordinary arrangement of organs (Dictionary). Situs inversus is when the organs in the chest and abdomen are mirrored, or opposite, of where their ordinary location should be. This is a unique genetic condition that affects 1 in 10,000 babies born each year (“15 Incredible Situs Inversus Statistics”). While situs inversus is the general term used, there are three subtypes of the condition that can occur: dextrocardia, levocardia and ambiguous.

A genetic disorder is a genetic condition, originally caused by a DNA abnormality. Genetic disorders can be inherited or can form early, in the development of child’s womb. Marfan syndrome is a genetic disorder that affects the body’s connective tissues in many parts of the human body. These specific connective tissues are made with the help of fibrillin, to produce elastic fibers, which are essential for connective tissues. The connective tissues are the tissues that provide strength and flexibility to many structures such as the bones, blood vessels, ligaments, muscles, and heart vessels. Connective tissues also allow the body to grow and develop properly. Marfan syndrome occurs when there is a mutation in the gene, specifically what tells

A genetic disorder, such as DiGeorge syndrome, is an illness caused by one or more abnormalities, which can be passed down through parents, DNA, or mutations. DiGeorge syndrome (DGS) is a rare type of a genetic disorder which is caused by the deletion of chromosome 22. DiGeorge syndrome affects many parts of the body and has a prevalence of 1: 4000

People with the genetic condition have distinctive facial features, experience sleep problems, feeding issues, growth and developmental delays. The 5-year-old also has branch pulmonary stenosis, which is a heart condition.

Across the planet, four times every second, a new human is conceived. In just nine months, a single cell no bigger than a speck of dust transforms into the most complex organism on earth. There are many events that shape and define us long before we’re born. Right from the start, it’s a journey full of surprises. There are many things that make you who you are today.

Throughout this discovery process there have been many questions that have guided the scientific community towards finding answers. One of the earlier questions was “how does the embryo take form and differentiate to become an organised organism?”