Sep 18, 2017 · 10 Most Interesting and Extremely Rare Genetic Disorders.One big factor, however, is the environment. Things like radiation exposure or other pollutants such as cigarette smoke, can result in genetic mutations, and 1 in 10 Americans are affected by rare diseases according to Global Genes. The organization also says there are different rare genetic disorders affecting people all over the world. Here is a list of the top 10 genetic disorders which are most common and prevalent world wide:Familial combined hyperlipidemia.Familial hypercholesterolemia.Dominant otosclerosis.Adult polycystic kidney disease.Multiple exostoses.Huntington’s disease.Fragile X-syndrome. Proteus Syndrome is a rare genetic disorder in which bones, skin, and other tissues are overgrown. The disorder results from a mutation in a gene called AKT1 which controls cell growth. In this disorder, some of the cells grow and some don't. This difference in the sizes of cells causes the overgrowth. The 16 Most Common Genetic Diseases Cystic Fibrosis. Cystic fibrosis CF is among of the most common inherited diseases in Caucasians.Down syndrome. Down syndrome is a common chromosomal abnormality caused by an extra copy.Fragile X syndrome. Fragile X syndrome is associated with the most.

Start studying Ch 10 Genetic Disorders. Learn vocabulary, terms, and more with flashcards, games, and other study tools. Top Ten Worst Genetic Diseases.Research is ongoing to detect and treat genetic disease. The decision to be tested for genetic disease is often difficult and includes many moral and ethical issues. Genetic makeup passed on from parents and grandparents affects a person's life and the life of their own children. The worst genetic diseases are incurable.

Symptoms of the following disorders may be similar to those of Chromosome 10, Distal Trisomy 10q. Comparisons may be useful for a differential diagnosis: Chromosome 10, Monosomy 10p is a very rare chromosomal disorder in which the end distal portion of the short arm p of one chromosome 10 is missing deleted or monosomic. Cystic fibrosis is a serious genetic disorder that affects many organs e.g. lung and pancreas. It commonly leads to reduced bone mineral density, known as osteoporosis, which increases the likelihood of fractures. The short-term and long-term effects of fractures e.g.. Description.Two copies of chromosome 10, one copy inherited from each parent, form one of the pairs. Chromosome 10 spans more than 135 million DNA building blocks base pairs and represents between 4 and 4.5 percent of the total DNA in cells. Identifying genes on each chromosome is an active area of genetic research. 10 Unusual Genetic Mutations in Humans 1. Progeria. This genetic disorder is as rare as it is severe.2. Uner Tan Syndrome. Uner Tan syndrome is a somewhat controversial condition,.3. Hypertrichosis. Hypertrichosi s is also called "werewolf syndrome" or Ambras syndrome,.4. Epidermodysplasia.

A genetic disorder is a genetic problem caused by one or more abnormalities formed in the genome. Most genetic disorders are quite rare and affect one person in every several thousands or millions. [citation needed] The earliest known genetic condition in a hominid was in the fossil species Paranthropus robustus, with over a third of individuals displaying Amelogenesis imperfecta.

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