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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& Sex Sterile Female Sterile Male 3. TURNER SYNDROME This extra genetic material causes the developmental changes and physical features of Down syndrome. You can change your ad preferences anytime. We use your LinkedIn profile and activity data to personalize ads and to show you more relevant ads. 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. Carcinoid Syndrome may … Turner Syndrome Overview; What Is It? By: Mostafa Bakhshi 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 By: Mostafa Bakhshi Student Of Public Health Mashhad University Of Medical Scienses Iran-March 2015. If you continue browsing the site, you agree to the use of cookies on this website. Slideshare uses cookies to improve functionality and performance, and to provide you with relevant advertising. 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). As this eMedTV page explains, it only affects females. What is Down Syndrome 3. Group 2. Undeveloped testes, sparse […] Clipping is a handy way to collect important slides you want to go back to later. CONTENTS. 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. where chromosome 21 become trisomy. See our Privacy Policy and User Agreement for details. If you continue browsing the site, you agree to the use of cookies on this website. Turner syndrome • Turner syndrome (TS): is a genetic condition that only affects females. We use your LinkedIn profile and activity data to personalize ads and to show you more relevant ads. Down syndrome typically is recognized at birth, Turner syndrome often is not recognized until adolescence,and many men with Klinefelter syndrome are never diagnosed. 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]. 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. The incidence of Down syndrome is 1 in 700 newborns, while the incidence of Turner syndrome is 1 in 5,000 births. • 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). 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 … Clipping is a handy way to collect important slides you want to go back to later. Turner syndrome is a chromosomal disorder that affects only females. Down Syndrome occurs in a fetus with a full or partial extra copy of Chromosome 21, with characteristic features, congenital anomalies, hypotonia & Intellectual Disability. Student Of Public Health TS was first described in the United States in 1938 by Dr. Henry Turner. Turner syndrome is characterized by complete or partial absence of one of the two X chromosomes. See our User Agreement and Privacy Policy. Down syndrome varies in severity, so developmental problems range from moderate to serious. Klinefelter syndrome is caused when a male baby is born with more than required or extra X chromosomes. Turner syndrome is the complete or partial monosomy of the X chromosome, which is characterized primarily by the hypogonadism in phenotypic females. 1. In this condition, there is missin… Muni Venkatesh. March 2015. Introduction. what is the difference between down syndrome and turner syndrome? It is believed 99% of all 45,X conceptions result in miscarriage. Down syndrome is caused by an extra or part of an extra 21st chromosome while. 49 years experience Developmental and Behavioral Pediatrics. 49 years experience Developmental and Behavioral Pediatrics. Turner Syndrome . Both are caused by : genetic accidents. Children with LGS have seizures often, and they have several different kinds of seizures. Turner syndrome is also known as monosomy of the X chromosome. 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. It is caused by a partial or complete absence of one of the X chromosomes in a female. Overview and Key Difference 2. Genotype 44 + X0 44 + XXY 2. P 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. Learn vocabulary, terms, and more with flashcards, games, and other study tools. Down syndrome, Turner syndrome, and Klinefelter syndrome constitute the most common chromosomal abnormalities encountered by primary care physicians. No public clipboards found for this slide. 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 … For example, it may be helpful to know that: Treating NETs does not necessarily treat Carcinoid Syndrome. 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 [1][2][3] … The missing genetic material … Individuals with this syndromes are phenotypically males but with tendency towards femaleness. ... Klinefelter syndrome, Turner syndrome, and Down syndrome are caused by chromosomal mutations. Since there is usually one … Now customize the name of a clipboard to store your clips. Learning the difference between NETs and Carcinoid Syndrome can help you have an informed discussion at your next appointment. Slideshare uses cookies to improve functionality and performance, and to provide you with relevant advertising. Down syndrome is the most common genetic cause of learning disabilities in children. Down syndrome causes a distinct facial appearance, intellectual disability, developmental delays, and may be associated with thyroid or heart disease in a person. Sex Characters Undeveloped ovaries and breasts, small uterus, absence of menstruation, absence of sex chromatin, narrow hips. This syndrome is found in 1 out of 1000 males. Turner Syndrome occurs in a female fetus with an incomplete or missing X Chromosome, with characteristic features, … 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 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 This page further explores this syndrome and its causes, symptoms, and treatment options. 1. Dr. Johanna Fricke answered. 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. 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. Lennox-Gastaut syndrome is a rare and severe kind of epilepsy that starts in childhood. 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. Now customize the name of a clipboard to store your clips. Looks like you’ve clipped this slide to already. 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. 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