You can change your ad preferences anytime. Difference betweeen Klinefelter Syndrome and Turner Syndrome Klinefelter in 1942 reported an abnormal male syndrome, which came to be known as Klinefelter syndrome . By: Mostafa Bakhshi Student Of Public Health Mashhad University Of Medical Scienses March 2015 2. As stature and sexual development are the two main characteristics of TS, the condition may go undiagnosed until a girl reaches school age or puberty.As stature and sexual development are the two main characteristics of TS, the condition may go undiagnosed until a girl reaches school age or puberty.As stature and sexual development are the two main characteristics of TS, the condition may go undiagnosed until a girl reaches school age or puberty. If you continue browsing the site, you agree to the use of cookies on this website. Turner syndrome (TS) is a chromosomal condition that describes girls and women with common features that are caused by complete or partial absence of the second sex chromosome. Start studying Turners Syndrome vs Down Syndrome. Down syndrome typically is recognized at birth, Turner syndrome often is not recognized until adolescence,and many men with Klinefelter syndrome are never diagnosed. Down syndrome is caused by an extra or part of an extra 21st chromosome while Turner syndrome is caused by an absence in one or part of the sex(X) chromosome.Down syndrome can occur in … Down syndrome causes a distinct facial appearance, intellectual disability, developmental delays, and may be associated with thyroid or heart disease in a person. ... Klinefelter syndrome, Turner syndrome, and Down syndrome are caused by chromosomal mutations. Turner syndrome is named for Dr. Henry Turner, who in 1938 published a report describing the disorder. What is Down Syndrome 3. It is caused by a partial or complete absence of one of the X chromosomes in a female. Now customize the name of a clipboard to store your clips. No public clipboards found for this slide. Turner Syndrome Overview; What Is It? The main difference between gene mutation and chromosomal mutation is that gene mutation is an alteration of the nucleotide sequence of a gene whereas chromosomal mutation is an alteration of the structure or number of chromosomes. If you continue browsing the site, you agree to the use of cookies on this website. Lennox-Gastaut syndrome is a rare and severe kind of epilepsy that starts in childhood. Down syndrome is the most common genetic cause of learning disabilities in children. Mashhad University Of Medical Scienses Sex Characters Undeveloped ovaries and breasts, small uterus, absence of menstruation, absence of sex chromatin, narrow hips. Now customize the name of a clipboard to store your clips. No public clipboards found for this slide. In this condition, there is missin… 3 ARDS is fairly common and has high mortality • 10% of all ICU patients and 23.4% of all patients with Mechanical Ventilation in ICU • Overall hospital mortality- 40% • ARDS Period Prevalence: Mild - 30%, Moderate - 46.6% and Severe -23.4% and hospital mortality progressively increases Overview and Key Difference 2. See our Privacy Policy and User Agreement for details. Clipping is a handy way to collect important slides you want to go back to later. Slideshare uses cookies to improve functionality and performance, and to provide you with relevant advertising. You can change your ad preferences anytime. In 75-80% of cases, the single X chromosome comes from the mother's egg; the father's sperm that fertilizes the egg is missing its sex chromosome. Both are caused by : genetic accidents. Klinefelter syndrome is caused when a male baby is born with more than required or extra X chromosomes. Down syndrome, Turner syndrome, and Klinefelter syndrome constitute the most common chromosomal abnormalities encountered by primary care physicians. TURNER SYNDROME BY OMOTAYO ADESIYUN OTHER NAMES Ullrich-Turner syndrome Monosomy X INCIDENCE One of the most common mosomies Incidence is 1/2500 liveborn females ... – A free PowerPoint PPT presentation (displayed as a Flash slide show) on PowerShow.com - id: 3cff65-M2ZhM It results when a female's cells have one normal X chromosome and the other sex chromosome is either missing or structurally altered (females without Turner syndrome have two normal X chromosomes in each cell, and males have one X and one Y chromosome).Signs and symptoms may include short … Turner syndrome leads to various developmental problems and people with this syndrome are at risk of many diseases. 1. 1. It is a chromosomal condition describing girls and women with common features, physical traits and medical conditions caused by the complete or partial absence of the second sex chromosome. The incidence of Down syndrome is 1 in 700 newborns, while the incidence of Turner syndrome is 1 in 5,000 births. Learning the difference between NETs and Carcinoid Syndrome can help you have an informed discussion at your next appointment. Children with LGS have seizures often, and they have several different kinds of seizures. Both are caused by : genetic accidents. We use your LinkedIn profile and activity data to personalize ads and to show you more relevant ads. 49 years experience Developmental and Behavioral Pediatrics. TURNER SYNDROME Slideshare uses cookies to improve functionality and performance, and to provide you with relevant advertising. Turner syndrome 1. The main difference between Klinefelter and Turner syndrome is that Klinefelter is a condition of trisomy in which one extra X chromosome is present in the genome of the person and Turner syndrome is a condition of monosomy in which one X chromosome is lacking in the genome of … Turner Syndrome and Down Syndrome Diagnosing Turner's Turner Syndrome Down Syndrome Three Types of Down Syndrome Most common chromosomal anomaly Incidence of 1 in 600 or 1 in 900 live births Newborns puffy hands and feet redundant nuchal skin suspected if edema or hypoplastic Group 2. Student Of Public Health See our Privacy Policy and User Agreement for details. Sex Sterile Female Sterile Male 3. See our User Agreement and Privacy Policy. Turner syndrome is the complete or partial monosomy of the X chromosome, which is characterized primarily by the hypogonadism in phenotypic females. The key difference between Down syndrome and Edward syndrome is that Down Syndrome is caused by the presence of an extra copy of chromosome 21 whereas Edward Syndrome is caused by the presence of an extra copy of chromosome 18. Turner syndrome is a chromosomal disorder that affects only females. Diagnosis(of(Fragile(X(and(Turner’s(Syndrome(Kevin&Miller&(kjmiller@stanford.edu)& && Dilli&Raj&Paudel&(drpaudel@stanford.edu)& CS&229&Machine&Learning&Final&Project& 1. Turner syndrome occurs in 1/2500 live births. Turner Syndrome
By: Mostafa Bakhshi
Student Of Public Health
Mashhad University Of Medical Scienses
Iran-March 2015. 46XY complete gonadal dysgenesis (SWYER SYNDROME) is a rare type of Disorder of Sex Development (DSD) first described by Gim Swyer in 1955 where a 46-XY subject presents with internal and external female genitalia, normal or little mammary development and primary amenorrhoea, without clinical stigmata for Turner syndrome. By: Mostafa Bakhshi 49 years experience Developmental and Behavioral Pediatrics. Turner syndrome can cause symptoms and complications throughout life, but treatments allow girls and women with this rare genetic disease to live relatively healthy lives. Key Difference – Klinefelter vs Turner Syndrome Klinefelter syndrome is defined as the male hypogonadism that occurs when there are two or more X chromosomes and two or more Y chromosomes. ADVERTISEMENTS: Some of the major Differences between Turner’s syndrome and Klinefelter’s Syndrome are as follows: Character Turner’s Syndrome Klinefelter’s Syndrome 1. Slideshare uses cookies to improve functionality and performance, and to provide you with relevant advertising. Answer: down syndrome is an autosomal disease. Clipping is a handy way to collect important slides you want to go back to later. Turner syndrome • Turner syndrome (TS): is a genetic condition that only affects females. It is believed 99% of all 45,X conceptions result in miscarriage. It involves a lack of part or all of a second sex chromosome in some or all cells. Down syndrome is a chromosomal abnormality characterized by the presence of an extra copy of genetic material on chromosome 21, either in whole (trisomy 21) or part (such as due to translocations).The effects of the extra copy varies greatly from individual to individual, depending on the extent of the extra copy, genetic background, environmental factors, and random chance. [1][2][3] … The missing genetic material … Turner syndrome (TS) occurs in approximately one out of every 2,000- 4,000 female live births. Dr. Johanna Fricke answered. A single X chromosome is the most common cause of miscarriage. Turner syndrome is caused by an absence in one or part of the sex(X) chromosome. This page further explores this syndrome and its causes, symptoms, and treatment options. Women with Turner syndrome appear to have a stocky appearance, arms that turn out slightly at the elbow, a receding lower jaw, a short webbed neck, and low hairline at the back of the neck. Down syndrome varies in severity, so developmental problems range from moderate to serious. Introduction. This extra genetic material causes the developmental changes and physical features of Down syndrome. Down Syndrome occurs in a fetus with a full or partial extra copy of Chromosome 21, with characteristic features, congenital anomalies, hypotonia & Intellectual Disability. Carcinoid Syndrome may … P and turner syndrome is a sex chromosomal disorder where 46 XO condition present.. Post Answer and Earn Credit Points Get 5 credit points for each correct answer. Down syndrome varies in severity among individuals, causing lifelong intellectual disability and developmental delays. where chromosome 21 become trisomy. Down syndrome, Turner syndrome, and Klinefelter syndrome constitute the most common chromosomal abnormalities encountered by primary care physicians. Down syndrome is caused by an extra or part of an extra 21st chromosome while. Down syndrome is a genetic disorder caused when abnormal cell division results in an extra full or partial copy of chromosome 21. What is Edward Syndrome 4. Turner syndrome is a chromosomal disorder that affects development in females. CONTENTS. Looks like you’ve clipped this slide to already. These can be explained by saying that both the terms are problems related to the sex chromosomes, as in the earlier one there is lacking of one of the sex chromosomes and so-called as monosomy (2n-1), while the latter consist of the extra sex chromosome and so-called as trisomy (2n+1). Increased understanding of Down syndrome and early interventions make a big difference in the lives of both children and adults with Down syndrome See our User Agreement and Privacy Policy. We use your LinkedIn profile and activity data to personalize ads and to show you more relevant ads. If you continue browsing the site, you agree to the use of cookies on this website. Turner Syndrome occurs in a female fetus with an incomplete or missing X Chromosome, with characteristic features, … 1. Down syndrome is caused by an extra or part of an extra 21st chromosome while Turner syndrome is caused by an absence in one or part of the sex(X) chromosome.Down syndrome can occur in … Turner syndrome is also known as monosomy of the X chromosome. Turner syndrome is characterized by complete or partial absence of one of the two X chromosomes. If you continue browsing the site, you agree to the use of cookies on this website. As this eMedTV page explains, it only affects females. This syndrome is found in 1 out of 1000 males. Looks like you’ve clipped this slide to already. TS was first described in the United States in 1938 by Dr. Henry Turner. Learn vocabulary, terms, and more with flashcards, games, and other study tools. Turner Syndrome . what is the difference between down syndrome and turner syndrome? The coexistence of double aneuploidy is very rare; Down-Turner published reports showed mosaicism related to two or more cell lines; the first case was reported in 1971 [1–3]. Individuals with this syndromes are phenotypically males but with tendency towards femaleness. For example, it may be helpful to know that: Treating NETs does not necessarily treat Carcinoid Syndrome. Turner syndrome is the dysgenesis in the female gonads, while Klinefelter syndrome is the male hypogonadism. Genotype 44 + X0 44 + XXY 2. Muni Venkatesh. Slideshare uses cookies to improve functionality and performance, and to provide you with relevant advertising. March 2015. Since there is usually one … • The condition is caused by an abnormal chromosome and affects about one in every 2,500 baby girls, but is much more common among pregnancies that do not survive to term (miscarriages and stillbirths). The fetuses are often severely hydropic (Figure 1). Undeveloped testes, sparse […] Difference between down syndrome is the most common cause of learning disabilities in.. What is the complete or partial monosomy of the sex ( X ).! 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