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Sindrome 44 xo. Age does not play any role d.
- Sindrome 44 xo. Most commonly, the affected female has only one X chromosome (45XO); others may have two X chromosomes, but one of them is incomplete (Turner mosaicism). Patients are phenotypically female and have short stature, webbed neck, widely spaced nipples, and gonadal dysgenesis. Turner's syndrome is a condition where a female is partly or completely missing an X chromosome, resulting in a 45,XO karyotype. It is also known as 45, X, or 45, XO due to the missing part of the XX chromosome. Super female = 44 + XXX Turner's syndrome is the genetic disorder where a single fragment or entire sex chromosome is missing. The female suffering from Turner syndrome is short-statured and sterile having a rudimentary ovary (not well developed), underdeveloped breast, and lack of other secondary sexual characteristics. Which one of the following conditions in humans is correctly matched with its chromosomal abnormality or linkage? Erythroblastosis fetalis - X linked Down syndrome - 44 autosomes + XO Klinefelter syndrome - 44 autosomes + XXY Colour blindness - Y Iinked Which one of the following condition in humans is correctly matched with its chromosomal abnormality/linkage? Erythroblastosis foetalis - X-linked Down syndrome - 44 autosomes + XO Klinefelter's syndrome - 44 autosomes + XXY Color blindness - Y-linked Nov 10, 2024 · Solution For SUBMIT (II) 00:22:01 Botany INSTRUCTIONS 134 Negative Marks 4. Trisomy is the gain of an extra chromosome (2n+1). A human male with Klinefelter’s syndrome, 44+XXY/ 44+XXXY/ 44+XXXXY, can have 1, 2 or 3 Barr bodies, depending on the number of X-chromosome. Everyone’s experience is different, and some health concerns may not show up until later in life. This fact sheet describes the chromosome condition Turner syndrome and includes the symptoms, cause and any treatment or testing which is available. So, this option is the correct one as it occurs due to monosomy (2n-1) ; the individual has 2n =45 chromosomes with 44 + XO genotype. Identify the person who suffers from Klinefelter's syndrome? Write the symptoms. 1 out of 1000 males have this syndrome. Learn about Turner's Syndrome, its symptoms, and how it differs from other genetic conditions. Learn about the types, symptoms, diagnosis, and treatment. Due to varied phenotypical presentation, the diagnosis of TS can create a spectrum of clinical เป็นภาวะที่พบว่ามีความผิดปกติของโครโมโซมที่มีผลต่อการพัฒนาในเพศหญิง โดยมีการขาดหายไปของโครโมโซมเพศ จำนวน 1 แท่ง (XO) ซึ่งอัตราการพบนั้นอยู่ Turner Syndrome - Learn about the causes, symptoms, diagnosis & treatment from the Merck Manuals - Medical Consumer Version. Old age of the mother c. Over 90% of the pure XO conceptuses are eliminated during prenatal development and postnataly, chromosomal mosaicism of both X and Y chromosomes are observed. These diverse Different chromosomes number of same human beings ABC and D are given below : A) 22 pairs of Autosomes B) 22 pairs of Autosomes + XO C) 22 pairs of Autosomes + 1 Autosome D) 22 pairs of Autosome + XXY. Turner syndrome is treated using hormonal replacement therapy. Such females are sterile and have short stature webbed neck broad shield-shaped chest etc. It is caused by the absence of all or part of the second sex chromosome. 2 Very Short Answer Questions. Klinefelter disorder is portrayed by the presence of an extra (at least one) X chromosome in male people, giving a 47, XXY as opposed to 46, XY karyotype. - In Turner Syndrome, individuals typically have 44 autosomes and only one X chromosome (XO). A sex chromosome abnormality that involves the presence of one functional X chromosome and no other X or Y chromosome Turner syndrome 45,XO gonadal dysgenesis A chromosomal abnormality with karyotype 45,XO. Also known as XO syndrome or ovarian short-stature syndrome. Aug 5, 2016 · WHAT IS IT? Also known as 45,X ; monosomy X; Turner’s syndrome; Ullrich-Turner syndrome. Therefore the karyotype of a person with Klinefelter's syndrome would be 44 + X X Y. Turner syndrome is a condition of females who, in the classic form, carry only a single X chromosome (45,X Connecting 44 + XO to the Correct Disorder Based on the analysis above: Down's Syndrome involves an extra autosome (chromosome 21), not a sex chromosome abnormality. (a) XO (b) XY (c) XXY (d) XX (III) The incidence of Down’s syndrome increases with maternal age, and not significantly with paternal age. Learn about mosaic Turner syndrome (TS), a genetic condition that affects growth and development in women and girls. Individuals are female with limited secondary sex characters, rudimentary ovaries, short statures, webbed skin over the neck, etc. Turner syndrome (TS) is a genetic condition occurring predominantly in girls and women. male adult with structurally abnormal Y chromosome This set of Class 12 Biology Chapter 5 Multiple Choice Questions & Answers (MCQs) focuses on “Inheritance and Variation Principles – Chromosomal Disorders”. Explore symptoms, inheritance, genetics of this condition. These patients are chromatin-negative. When some cells only contain an X, the 45,X/46,XY condition arises. Females have two X chromosomes (46, XX), and males have one X and one Y chromosome (46, XY). Which of the following is the carrier of genetic information? a) Proteins b) Amino acids c) Carbohydrates d) DNA View Answer. The common genetic explanation for the early lethality of monosomy X embryos, as well as the phenotype of surviving individuals is Find the mismatch pair: a. They are sterile feminised males with enlarged breasts and exhibits a eunuchoid body habitus (tall and thin). org 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). Exercise 8. Turner Syndrome The typical female karyotype (“sex” chromosome make-up) for females is 46,XX. Barr bodies will not be present in human females affected with Turner's syndrome. Phenotypically these individuals are females but ovaries are rudimentary and always sterile. So the type of individual with Turner's syndrome is 44 A + XO So, the correct answer is option C. Identifying the Condition: The condition characterized by 45 chromosomes (44 + XO) is associated with Turner syndrome. Treatment can help manage symptoms. 50% d. The condition results in short height, underdeveloped ovaries and heart defects. In a person with Turner Syndrome, female sex characteristics are XO syndrome is a disorder of the sex chromosomes, occurring in females, in which one of the two X chromosomes is completely or partially absent. Turner syndrome leads to various developmental problems and people with Turner syndrome are at risk of many diseases. These include XY-Turners, mosaic XY/XO and XO/XY. Turner's Syndrome is monosomy caused by absence of one copy of X-chromosome from females and is donated by 44 +XO or 45X. Turner's syndrome is also referred to as 45,X, because a normal, healthy individual has 46 chromosomes, 44 autosomes and 2 sex chromosomes. This condition is known as Turner Syndrome. It is marked by the presence of one or more extra X chromosomes in the individual (44+XXY/ 44+XXXY/ 44+XXXXY). Downs syndrome is due to the trisomy of 21st pair of chromosome. Since the single X chromosome is maternally derived in 80%, the genesis of the 45,X karyotype is due Human genetic disease - Sex Chromosome Abnormalities: About 1 in 400 male and 1 in 650 female live births demonstrate some form of sex chromosome abnormality, although the symptoms of these conditions are generally much less severe than are those associated with autosomal abnormalities. It occurs in about 1 / 2,000 live female births: a large proportion of monosomic X fetuses are aborted spontaneously in the first trimester. In the long Sep 24, 2013 · Turner syndrome is a chromosomal condition that alters development in females. The most common chromosomal finding in Turner’s syndrome is 44 autosomes and only one X chromosome. A colourblind man marries a woman who is homozygous for normal colour vision, the probability of their son being colourblind is - a. Turner syndrome (TS) is the most common cause of short stature and delayed puberty in females. Many The presence of one or more extra copy of X-chromosome in males causes Klinefelter Syndrome. Down’s syndrome = 44 + XY, b. Turner syndrome is also known as monosomy of the X chromosome. Symptoms of Turner A rare chromosomal anomaly syndrome characterized by complete or partial loss of an X chromosome in phenotypic females, clinically manifesting with short stature, primary ovarian insufficiency as well as cardiovascular, renal, liver, autoimmune diseases, hearing loss and neurocognitive abnormalities. It only happens in people assigned female at birth (AFAB). Ans: Hint: It is a genetic disorder in males. The X chromosome that is inherited can be either maternal or paternal, although it is usually maternal in origin. Jul 25, 2022 · What Is the Karyotype of Turner Syndrome? The karyotype seen in an individual with Turner's syndrome is 44 A + XX, 45 A + XY, 44 A + XO, and 44 A + XXY. To solve the question, we will identify the disorders associated with the given genotypes and provide two symptoms for each disorder. Last option is D which is Klinefelter's syndrome. , 44+XO instead of having 46 chromosomes. This female lacks the second X chromosome present in the normal karyotype. Ans: Hint: Males with jacob syndrome have 47 chromosomes because of the extra Y chromosome. Girls with TS are shorter than most girls. Turner syndrome (TS) is a complex developmental disorder in individuals with short stature who possess a 45,X cell line, with or without mosaicism. The resulting young one is an abnormal sterile male. Turner syndrome is associated with many additional abnormalities, including infertility, coarctation of the aorta, horseshoe kidney, and osteoporosis. The affected individual has 44+ XXY /44+XXXY / 44+XXXXY chromosomes. Turner syndrome (44+XO) is an example of monosomy in humans. Es posible que, para algunas niñas, la presencia del síndrome de Turner no sea claramente evidente, pero para otras niñas, varias características físicas son evidentes desde el principio. This condition is also sometimes called Jacob's syndrome, XYY karyotype, or YY syndrome. Turner's syndrome karyotype 45,XO. They are sterile feminised males with enlarged breasts (Gynecomastia). Explain the statements : a. XO syndrome causes a number of symptoms that vary greatly among individuals, but generally include small stature, amennorhea and infertility. This means that the typical female has 46 chromosomes including two that look like X’s. Young age of the mother b. These symptoms are often noticed only at puberty, although this is one of the most common chromosomal disorders. Jun 19, 2023 · A female suffering from Turner's syndrome has 45 chromosomes with genotype 44+XO. Often, a short and webbed neck, low-set ears, low hairline at the back of the neck, short stature, and swollen hands and feet are seen at birth. Klinefelter's Syndrome involves an extra X chromosome (XXY), which is different from XO. Which chromosome condition is Jacob syndrome? (a)44+XO (b)44+XXY (c)44+XYY (d)45+YY4. Complete answer: Klinefelter's condition otherwise called 47 + XXY or XXY Genotype of Down’s syndrome isA) 45 + XXB) 44 + XYC) 44 + XXYD) 22 + XY. In Turner Syndrome, which encompasses several conditions, cells are missing all or part of an X chromosome. So, the genetic composition in these females is 44 + XO. In persons with Turner's syndrome, there is a single X chromosome (44 +XO). On rare occasions, chromatin-negative patients with gonadal dysgenesis have a male sex chromosme constitution (46/XY). Klinefelter syndrome = 44 + XXY d. This makes option B Feb 9, 2018 · The human genome is diploid (2n), consisting of 44 autosomes and two sex chromosomes. They lack a barr body as they have only one X-chromosome. So, the correct answer is 'Turner's syndrome'. Turner's Syndrome is characterized by the absence Understand the genetic disorder associated with a 44 + XO karyotype. 100% Q. [10] The complications commonly include infertility and small, poorly functioning testicles (if present). [1][2] The person is generally otherwise normal, including typical rates of fertility. Females with turner’s syndrome have 44+XO chromosomes and the number of chromosomes is 45. At 44 feet, the EXPLR really benefits from the rigidity attainable by aluminum with sturdy 8mm stringers at the bottom and a 5mm hull. Karyotype of Turner’s Syndrome 4. They don’t go through normal puberty as they grow into adulthood. Vibrations and shatters from rough seas just vanish and the solid seaworthiness can be felt at the wheel of this ultimate exploration yacht. The common genetic explanation for the early lethality of monosomy X embryos, as well as the phenotype of surviving individuals is What is Turner syndrome (TS) in children? Turner syndrome (TS) is a genetic disorder that occurs in girls. Was this solution helpful? Feb 11, 2022 · Los signos y síntomas del síndrome de Turner pueden variar entre las niñas y mujeres que padecen el trastorno. The genotype of Turner’s syndrome is represented by (44 + XO). Klinefelter syndrome (44+XXY/XYY) and Down syndrome are the examples of trisomy. In normal females there is a presence of 44+XX chromosomes but due to this disease, they have 45 chromosomes i. Klinefelter syndrome = 44+ XX Y d. ii 44 with XO chromosomes - such females are sterile as ovaries are rudimentary. Aug 28, 2024 · Turner syndrome (TS) results from the loss of one X chromosome in phenotypic females, leading to a range of complications such as short stature, cardiovascular issues, autoimmune disorders, metabolic imbalances, osteoporosis, neurocognitive deficits, hearing loss, abnormalities in endocrine functions, infertility, disruptions in bone metabolism, and neurocognitive deficits. In this, a male baby is born with one extra X chromosome. If a married couple has a baby with Down’s syndrome, what will be the possible reason for the condition? a. Because TS can affect Jun 27, 2023 · Turner syndrome is a rare condition caused by an abnormal sex chromosome in a person assigned female at birth. Identify the Genotype 44 + XO: - The genotype 44 + XO indicates a missing X chromosome in females. However Turner syndrome is found in female which genotype has 45 number of chromosome such as 44+XO Turner syndrome (TS), also called monosomy x, is a genetic condition where one of the X chromosomes is missing or partly missing. Therefore, the correct answer is option A. They may also have other health problems, such as heart or kidney problems. Los signos y síntomas pueden ser sutiles y desarrollarse lentamente con el tiempo, o A Colour blindness- Y linked B Erythroblastosis fetalis- X linked C Down syndrome- 44 autosomes+XO D KIinefelter's syndrome- 44 autosomes+XXY Views: 817 students Klinefelter's syndrome also known as 47 + XXY or XXY (44 autosomes and 3 sex chromosomes) is the set of symptoms that result from two or more X chromosomes in males. Typically, most people have 46 chromosomes in 23 pairs; 22 of these pairs are the same in both males and females. They have no barr body. The birth prevalence of KS in the State of Victoria, Australia These are sterile females with poorly developed ovaries, small uterus and underdeveloped breasts. Turner syndrome (TS), commonly known as 45,X, or 45,X0, [note 1] is a chromosomal disorder in which cells of females have only one X chromosome instead of two, or are partially missing an X chromosome (sex chromosome monosomy) leading to the complete or partial deletion of the pseudoautosomal regions (PAR1, PAR2) in the affected X chromosome See full list on mayoclinic. Klinefelter syndrome = 44 + XXY, d. Chromosomal formula is 44 + XO. Note:- Turner syndrome may be diagnosed before birth or shortly after birth or during early childhood filled stop however, in some cases the disorder may not be diagnosed until well into adulthood, often an incidental finding. from publication: CHROMOSOME STUDY IN SUSPECTED CASES OF TURNER'S SYNDROME FROM JAMMU REGION OF JAMMU & KASHMIR Klinefelter syndrome (or XXY syndrome) is a chromosome disorder that affects males. Learn about the symptoms and treatment here. Hence the correct option is 2. Turner's syndrome is correctly represented as 44 + XO (45 chromosomes). When there is a mistake in the formation of spe Turner Syndrome (X monosomy/XO females): It is a sex chromosomal disorder caused due to non-disjunction of chromosomes during gamete formation. When this gamete fertilizes a normal gamete containing one X chromosome, it results in an XO (the O means there is no second sex chromosome) female with only 45 chromosomes. A A- Turner's syndrome with 44+XO B-Klinefelter's syndrome with 44+XXY Correct option c Turners syndromeExplanationIn human beings 45 chromosomes/XO abnormality causes Turners syndrome. The individuals with the syndrome are sterile females with webbed necks. Down’s syndrome = 44 + XY b. The affected male has an additional X chromosome, which causes infertility and may cause the development of characteristics such as tall stature and breast development. When there has been a non-jusduction in the chromosome in meiosis, it is induced. Another Jul 21, 2023 · Step by step video & image solution for Identify the syndrome from the given below. 25% c. This is sometimes referred to as 45,XO or 45,X karyotype. It is also hence known as trisomy-21 and is represented as 45+XY or 45+XX. Down's syndrome = 44 +XY b. [1] The condition is generally Download scientific diagram | Karyotype of Turner Syndrome with Monosomy X (45, XO). The 44 autosome + XO condition is due to Turner s syndrome. Klinefelter’s syndrome (XXY Turner syndrome with 45, XO karyotype is the only monosomy of the X chromosome known to occur 1 in 2000–5000 female live births (Hook and Warburton, 1983). Complete answer: First we should know Down's syndrome is a genetic disorder where there is an extra 21st chromosome. Haemophilia is an X-linked gene mutation, not a numerical chromosome disorder like 44 + XO. The ovaries are reduced to fibrous streaks. Age does not play any role d. For the probability of a son 4 days ago · Turner Syndrome Turner syndrome is caused when nondisjunction produces a gamete with no sex chromosomes. 0% b. 2) Klinefelter’s Syndrome is characterized by a trisomy of the X-chromosome. [1] There are usually few symptoms. Using the expression 45,X/46,XY is probably best, most nearly accurate, and the least confusing. 44 Autosomes + XO by Biology experts to help you in doubts & scoring excellent marks in Class 12 exams. Sus características físicas son variadas. XO Abstract Turner's syndrome (caused by monosomy of chromosome X) is one of the most common chromosomal abnormalities in females. But in rare cases, a male is born with an extra X chromosome (XXY). ‘XO’-constitution is caused by non-disjunction more commonly in spermatogenesis than in oogenesis. e. Klinefelter syndrome is a sex chromosome disorder in boys and men that results from the presence of an extra X chromosome in cells. Unlike their human counterparts, XO mice are typically fertile, and their lack of a second sex chromosome can be transmitted from one generation to the next as an X-linked dominant trait with male Turner syndrome is a genetic disorder in females, it is due to the partial or complete loss of one of the X chromosomes. Males with XYY syndrome have 47 chromosomes because of the extra Y chromosome. Occurs in approximately 1:2500 births. Aug 21, 2024 · Turner syndrome is classically characterized by the absence of one X chromosome copy (45 XO), with the missing chromosome most frequently (two-thirds) being the paternal one. Hence the correct option is c. They have webbed neck and broad chest. Symptoms include short stature, neck wbbing, elbow deformity, widely spaced nipples with shield chest, primary amenorrhea, sexual infantilism and sterility. The condition has many different names. With XO EXPLR 44, our mission is to bring the premium material and naval architecture to adventure yachting. Turner syndrome happens in females when one X chromosome is missing or partially missing. Signs and symptoms vary among those affected. Ans: Hint: The genotype is Trisomy 21 for Down syndrome. Turner's syndrome = 44+ XO c. Tall stature, gynecomastia, small testis, disability in learning, and, at ti Which one of the following conditions in humans is correctly matched with its chromosomal abnormality/linkage? Colour blindness- Y linked Erythroblastosis fetalis- X linked Down syndrome- 44 autosomes+XO KIinefelter's syndrome- 44 autosomes+XXY Difference between Klinefelter’s and Turner syndrome What is difference between Klinefelter’s and Turner syndrome? Klinefelter syndrome is found in male which genotype has 47 number of chromosomes such as 44+XXY ( presence of one extra X chromosome) leading to symptom like sterility in male. Turner syndrome happens when a female is born with one missing or a partial X chromosome. 2. man or boy. This chromosomal issue can affect growth, heart health, fertility, and metabolism. The presence of extra copy of X-chromosome produces some feminine characters in otherwise male individuals. They have short stature (height) and webbed neck, lower posterior hair line, broad shield-shaped chest, poorly developed ovaries and breast, and low Turner's syndrome occurs due to a missing X chromosome in females. XYY syndrome, also known as Jacobs syndrome and Superman syndrome, is an aneuploid genetic condition in which a male has an extra Y chromosome. 00 1. Turner syndrome (TS) is the most frequently detected chromosomal abnormality in females caused by the partial or complete absence of second X chromosome. Jul 17, 2020 · In human beings 45 chromosomes (44+XO) causes: (a) Down Syndrome (b)Turner Syndrome (c) Edward Syndrome (d)Klinefelter Syndrome - 19653733 Individuals born with Turner’s syndrome have 44 autosomes with XO. Question 4. Test cross This abnormality occurs due to monosomy (2n - 1); the individual has 2n = 45 chromosomes with 44 + XO genotype Edward's syndrome Down's syndrome Turner's syndrome Klinefelter's syndrome Jun 6, 2023 · El síndrome de Turner (45, X0) está causado por una pérdida total o parcial de un cromosoma X en la mujer. They are phenotypically female. Dec 17, 2024 · Turner Syndrome (45 X Syndrome) Condition Description Turner Syndrome is caused by a missing sex chromosome. Approximately half of the patients have the classic form with a genotype of 45,XO, one-fourth of patients have different mosaic forms, and the remaining Which one of the following conditions in humans is correctly matched with its chromosomal abnormality/linkage? Klinefelter's syndrome - 44 autosomes + XXY Colour blindness - Y linked Erythroblastosis foetalis - X linked Down syndrome - 44 autosomes + XO An individual with 45 chromosomes and a 44 + XO genotype has Turner's syndrome. This is What is karyotype of feme in turner syndrome 45+xo or 44+ xo It is represented as 44 +XO. Find the mis match pair :- a. Super female = 44 + XXX The correct option is C 44 A + XO Turner syndrome (TS) or 45, X, is a condition in which a female is partly or completely missing an X chromosome. Father’s age is 11111 Fact Sheet 40| TURNER SYNDROME and any treatment or testing which is available. Klinefelter’s syndrome is an aneuploid trisomic disease. Although 3% of all pregnancies start with XO embryos, 99% of these pregnancies terminate spontaneously during the first trimester. Turner syndrome is a chromosomal condition that affects development in females. (b) Gradual accumulation in germ-line chromosomal mutations throughout reproductive age. Symptoms: They have a short stature (height) and webbed neck, a lower posterior hairline, a broad shield-shaped chest, poorly developed ovaries and breasts, and low intelligence. Give the Genotype of Turner’S Syndrome. Turner’s syndrome = 44 + XO c. i Turners syndrome. People with Turner syndrome have only one X chromosome present and fully functional. The individual has 2n = 45 chromosomes (44 + XO) instead of 46. Explore all Chromosomal Disorders related practice questions with solutions, important points to remember, 3D videos, & popular books. [2] These may include being taller than average and an increased risk of learning disabilities. The presence of an extra copy of X-chromosome produces some feminine characters in otherwise male individuals. 1. Klinefelter syndrome is a genetic condition where a male is born with an extra copy of the X chromosome. Thus they have 44 autosomes plus X chromosome. Individual born with Turner syndrome has 44 autosomes with XO. May 21, 2008 · The murine model for Turner Syndrome is the XO mouse. Klinefelter syndrome is correctly represented as 44 + XXY (47 chromosomes). Turner’s syndrome = 44 + XO, c. Other features include lack of other secondary sexual characters short stature and under developed feminine characters. 00 A person with Klinefelter's syndrome has 44 autosomes \\& xo sex ch Dec 4, 2022 · This abnormality occurs due to monosomy (2n - 1); the individual has 2n = 45 chromosomes with 44 + XO genotype - 54470554 Jul 5, 2020 · Find the mis match pair :- * 1 point a. Monosomy X (AKA Turner Syndrome) is a karyotypic condition caused by non-disjunction of X chromosomes at Meiosis I or II. However, a person with turner's syndrome has only 45 chromosomes, with the sex chromosome being an X chromsome. Aug 6, 2020 · Turner syndrome is a chromosomal disorder that is characterized by a missing or partially deleted X chromosome, resulting in a 45, XO female. Super female = 44+ XXX 9. The seriousness of these problems varies from girl to girl. Klinefelter’s Syndrome hasA)44+XXYB)44+XOC)45+XYD)66+XXY. Super female is correctly represented as 44 + XXX (47 chromosomes). What may reasonably explain this trend? (a) Failure of muscular contractions to correctly fuse the two gametes. The chromosome arrangement of Down syndrome is shown in figure 2. For the mismatch pair: Down's syndrome is caused by an extra chromosome 21 (Trisomy 21), so it should be 47 chromosomes in total, not 46 (44 + XY). Klinefelter syndrome (KS), also known as 47,XXY, is a chromosome anomaly where a male has an extra X chromosome. It causes many traits and problems. Henery H Turner first described this condition in 1938. In Turner syndrome, a female is born with a single X chromosome instead of the usual two sex chromosomes (XX). People typically have 46 chromosomes in each cell, two of which are the sex chromosomes. Hence the total number of chromosomes present in the affected individual = 44 autosomes + XXY. So, the correct answer is 'Loss of X chromosome - 44 + XO' Was this solution helpful? Hint: People with Klinefelter conditions are at expanded danger for bosom malignancy, immune system infections, diabetes, osteoporosis, and profound vein thrombosis. Jan 12, 2009 · Turner's syndrome (caused by monosomy of chromosome X) is one of the most common chromosomal abnormalities in females. ly4 n2pi d5p16 refkih5st 4ph7d vv0 kuczt 4wqsnr lm11 bbbzl