BY: Reilly Flodin & Alex Staffa

Slides:



Advertisements
Similar presentations
By: Liz Fleischer Period 3
Advertisements

Klinefelter’s Syndrome By Greg Schreck and Troy Krause
By: Ryan Wilding and Lukas Johnson
Genetic Diseases.
Turner Syndrome By: Olivia Hoefling.
Klinefelter's Syndrome & Turner’s Syndrome. Cause of Kleinfelter’s Male has extra Chromosome Known as XXY male Male has total of 47 chromosomes.
Numerical chromosome Aberrations
Klinefelter’s Syndrome
Klinefelter’s Syndrome
By: Little6CB18 and Little6CC3
NOTES 24 – Genetic Disorders and Hereditary Diseases
MUSCULAR DYSTROPHY By Jasmine DeLong. INHERITANCE Muscular dystrophy is a hereditary condition marked by progressive weakening and wasting of the muscles.
Introduction to Human Genetics. Facts Humans have 46 chromosomes or 23 pairs of chromosomes 2 types of chromosomes: –Autosomes: chromosomes that determine.
Chromosome Syndromes BY: Brandon and Kellen.
Genetic Disorders.
Chapter 4, Section 2 Human Genetic Disorders
Autosomal and Sex chromosome abnormalities
KARYOTYPING. 1.What is this? 2.How many chromosomes are in a human body cell? 3.How many pairs are in a human cell? 4.Which chromosomes determine gender.
14-2 Human Chromosomes.
Human Genetics – Studying Chromosomes & Diseases Biology.
What do you know about it?. Klinefelter Syndrome..that this particular birth defect is defined by the presence of an extra X chromosome in a male, and.
More Human Genetics… Biology. Multiple Alleles Traits are the result of more than 3 or more types of alleles Example: blood typing There are 3 different.
BY: Xavier Barnes.  Turner syndrome is a genetic condition that affects development in one in every 2,500 females. Turner Syndrome has a wide-range of.
Chromosomes & Karyotypes
Introduction to Genetics Genetics Terms Meiosis Nondisjunction disorders.
By Jayla Harris.   Turner syndrome is a disorder caused by the loss of genetic material from one of the sex chromosomes.  Turner syndrome (TS) is a.
Human Genes & Chromosomes. Human Genetic Disorders Nondisjunction is a cause of some human genetic disorders –In nondisjunction, the members of a chromosome.
1. CHROMOSOMES 2 CHROMOSOME NUMBER  All cells in the human body (SOMATIC CELLS) have 46 or 23 pairs of chromosomes  Called the DIPLOID or 2n number.
 A pair of sex cells fail to separate during the formation of an egg or sperm  Embryo ends up with three copies of chromosomes  (XXY)  A recessive.
1copyright cmassengale. Chromosomes 2 Chromosome Number All cells in the human body (SOMATIC CELLS) have 46 or 23 pairs of chromosomes Called the DIPLOID.
1. Chromosomes 2 Chromosome Number All cells in the human body (SOMATIC CELLS) have 46 or 23 pairs of chromosomes Called the DIPLOID or 2n number GAMETES.
By: GP. Medical Answers Q: How does a person inherit Klinefelter’s Syndrome? Is it dominant recessive, sex-linked, too many/ too few chromosomes, or a.
Klinefelter’s Syndrome
STARTER Now try your non-disjunction review sheet!
Human Genetics Biology.
Human Genetics Biology.
The chromosomal basis of inheritance provides an understanding of the pattern of passage (transmission) of genes from parent to offspring.
Chapter 14 The Human Genome Pg. 341.
Karyotypes.
Karyotypes. What is a karyotype? A karyotype is made from a picture of the nucleus of a cell which has begun to undergo mitosis. Mitosis is the process.
Pick up warm-up from front table. Complete warm-up first! Complete warm-up first! When finished…get out sponge bob worksheet. Do you have any questions???
Human Genetic Disorders Notes. What causes genetic disorders? Mutations, or changes in a person’s DNA.
A __________ is a picture of an organism’s chromosomes
Human Genetic Disorders Every cell in the human body has 46 chromosomes except for gametes, egg sperm cells, which contain 23 or the haploid number. Human.
Male and Female Reproductive System
NOTES 21 - Sex-Linked Inheritance
DNA and Mutations. 5 Mutation Facts Write down five facts about mutations as we go through the following videoclips Video 1 Video 2 – Repair Video 3 –
Meiosis and Chromosomal Inheritance. Chromosomes Karyotype – all chromosomes in an organism Homologous chromosomes – specific chromosome pair Gamete-
KAROTYPING CHROMSOME ABNORMALITIES. * Usually done from the 15th or 16th week to the 20 th week (2 nd trimester). *Only at this point in a pregnancy is.
Sex Determination & Nondisjunction Disorders June 13, 2016.
Complex Inheritance of Human Traits. Codominance With codominance, a cross between organisms with two different phenotypes produces offspring with a third.
Klinefelter Syndrome Santina King. Researched and developed by Dr. Harry Klinefelter - father of endocrinology Klinefelter syndrome is the occurrence.
Klinefelter’s? Syndrome? Klinefelter’s? Syndrome? Klinefelter’s? Syndrome? Klinefelter’s? Syndrome? Klinefelter’s?
Hypopituitarism By: Zach Lanham.
KLINEFELTER’S SYNDROME
Klinefelter syndrome 47xxy
Human Genetics part 2.
Turner Syndrome Ateo Ayiy.
Turner Syndrome By: Ann Steinhauser.
Biotechnologies: Assisted Reproduction Infertility and it’s Treatments
Atypical Cell Division
When Meiosis Goes Wrong:
Klinefelter syndrome 47,XXY
When Meiosis Goes Wrong:
By Abanoub Narouz and Omar Omar
Human Genetics – Studying Chromosomes & Diseases
Warm Up Complete Edpuzzle on pedigrees
Assisted Reproduction Infertility and it’s Treatments
Presentation transcript:

BY: Reilly Flodin & Alex Staffa Klinefelter Syndrome BY: Reilly Flodin & Alex Staffa This disorder is named after Dr. Harry Klinefelter who was the first to repot the symptoms in 1942

Inherited? Klinefelter (xxy) syndrome isn’t really inherited per say rather, it’s an accident where either an egg that already has 2 X alleles is fertilized by a regular sperm that has the Y allele, or a regular egg with one x allele is fertilized by a sperm with x and y alleles. About 1 in 750 males is affected by this disease, also it is almost never passed on, when cells are splitting to make sperm the problem is usually corrected by the cell

Diagnosis And Prognosis To diagnose this syndrome , which usually doesn’t appear until puberty, doctors look at the chromosomes of the person and they determine whether or not that person has an extra X chromosome Klinefelter’s syndrome has no effect on the life span of a person.

Symptoms & Treatments Infertility is the main problem with the xxy syndrome, the body just doesn’t produce nearly enough testosterone and too much estrogen to fully complete puberty correctly, this also can make the male start to grow breasts. The only very effective treatment is to take male hormones to stimulate normal male growth. Regular testosterone injections are often the treatment of choice for those with Klinefelter’s syndrome.

Everyday Life Most men with the help of treatment head on to lead normal and successful lives. Some men try not to use testosterone injections or pills and are infertile so they cannot have children of their own, also their bodies can resemble that of a woman’s. There will never be a true cure until it’s impossible to remove a whole chromosome, but treatment completely reverts the disorder so a cure may not be necessary Anyone seeking help for this problem can visit these pages or orginizations: klinefeltersyndrome.org/ The American Association for Klinefelter SyndromeInformation and Support(AAKSIS) www.aaksis.org/

These People have Klinefelter’s syndrome Interesting fact: there are variants of this disorder where there are multiple x alleles Ex: xxxy xxxxy xxxxxy all these of course are EXTREMELY rare