1. velo introduction

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1. velo introduction

  1. 1. INTRODUCTION TO GENETIC DISORDERSPresented By :Velo, John R.DMD2D
  2. 2. What is an Allele? an alternative form of a gene located at a specific position on a specific chromosome. These DNA codings determine distinct traits that can be passed on from parents to offspring. May be dominant or recessive The process by which alleles are transmitted was discovered by Gregor Mendel and formulated in what is known as Mendels law of segregation.
  3. 3. Difference between a dominant andrecessive allele If the two alleles from both parents are :  Similar : homozygous offsprings  Different : heterozygous the stronger of the two will show up in the offspring while the weaker one is masked
  4. 4. Difference between a dominant andrecessive allele Dominant Allele  A gene (allele) which is expressed clinically in the heterozygous state  In a dominant disorder, only one mutant allele need be present as it masks the normal allele Recessive Allele  A gene (allele) which is only expressed clinically in the homozygous state  can be suppressed if present with a dominant gene and will not show its character in presence of a dominant gene  Recessive alleles or genes will only show up if the offspring inherits recessive copies of the trait from both parents
  5. 5. Difference between a dominant andrecessive allele Dominant genes are usually the ones that are oftentimes observed in an offspring and passed down to subsequent generations while recessive genes will only show for a few generations and eventually disappear. Dominant genes are represented by capital letters and recessive genes are represented by small letters. There are three combinations of genotypes or alleles:  AA (receives dominant traits from both parents),  Aa (receives a dominant trait from one parent and a recessive trait from the other), and  aa (receives recessive traits from both parents)
  6. 6. What is a Punnett Square? a diagram that is used to predict an outcome of a particular cross or breeding experiment is visual representation of Mendelian inheritance
  7. 7. How is a trait transmitted?
  8. 8. Types of Genetic Disorders : Genetic disorder - disease caused by abnormalities in an individual’s genetic material (genome). The four different types of genetic disorders are :  (1) single-gene,  (2) multifactorial,  (3) chromosomal, and  (4) mitochondrial
  9. 9. (1) Single-gene (Mendelian ormonogenic) caused by changes or mutations that occur in the DNA sequence of one gene. Genes code for proteins, perform most life functions, and make up the majority of cellular structures. When a gene is mutated, its protein product can no longer carry out its normal function, a disorder can result. Some examples are cystic fibrosis, sickle cell anemia, Marfan syndrome, Huntington’s disease, and hereditary hemochromatosis.
  10. 10. Examples of Single-Gene Disorders B. A. C.A. Marfan’s SyndromeB. Cystic FibrosisC. Huntington’s Disease
  11. 11. (2) Multifactorial (complex orpolygenic) caused by a combination of environmental factors and mutations in multiple genes. Examples include heart disease, high blood pressure, Alzheimer’s disease, arthritis, diabetes, cancer, and obesity Multifactorial inheritance is also associated with heritable traits such as fingerprint patterns, height, eye color, and skin color.
  12. 12. (3) Chromosomal Chromosomes - distinct structures made up of DNA and protein, are located in the nucleus of each cell Because chromosomes are carriers of genetic material, such abnormalities in chromosome structure as missing or extra copies or gross breaks and rejoinings (translocations) can result in disease. Examples include Down syndrome or trisomy 21, Turner syndrome (45,X), Klinefelter syndrome (47, XXY) and cri du chat syndrome, or the "cry of the cat" syndrome (46, XX or XY, 5p-).
  13. 13. Examples of ChromosomalDisorders
  14. 14. (4) Mitochondrial This relatively rare type of genetic disorder is caused by mutations in the nonchromosomal DNA of mitochondria. Examples of mitochondrial disease include:  an eye disease called Lebers hereditary optic atrophy;  a type of epilepsy called MERRF which stands for myoclonus epilepsy with Ragged Red Fibers; and  a form of dementia called MELAS for mitochondrial encephalopathy, lactic acidosis and stroke-like episodes

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