Boys with 47, xyy syndrome have one x chromosome and two y chromosomes in. An xyy male with acute lymphoblastic leukemia, cancer. Ts and y sequences n26, and ts and ychromosome material n27. Pdf 47,xyy syndrome and male infertility researchgate. A diagnosis of xyy syndrome may be made before birth prenatally through amniocentesis or chorionic villus sampling. Genetic and rare diseases information center gard po box 8126, gaithersburg, md 208988126 toll free. Boys with 47, xyy syndrome have one x chromosome and. There is wide variability in the clinical presentation and prognosis of sexual chromosome anomalies. Read an xyy male with acute lymphoblastic leukemia, cancer genetics and cytogenetics on deepdyve, the largest online rental service for scholarly research with thousands of academic publications available at your fingertips. There are no fertility issues associated with xyy syndrome. A number of representative cytogenetic surveys were conducted years ago on newborns in various countries. If you have problems viewing pdf files, download the latest version of adobe reader. Nodulocystic acne as a phenotypic feature of the xyy genotype. Pdf living with klinefelter syndrome 47,xxy trisomy x 47,xxx and 47, xyy popular colection.
Jan 14, 2018 47, xyy syndrome is caused by having an extra copy of the y chromosome in each cell of the body. There are 47 chromosomes, instead of the usual 46, giving a 47,xyy karyotype. Investigations of the pattern of dna replication have shown that the x chromosomes in normal female cells exhibit marked asynchrony and one of them has a pronounced pattern of late replication. Oral, physical, and behavioral aspects of patient with. Clinical studies have suggested a poorer educational level and social adaptation among 47, xyy persons. Sindrome 47,xyy pediatria manuali msd edizione professionisti. Sex chromosome abnormalities scas turner syndrome ts 45,x, klinefelter syndrome ks 47,xxy, triple x syndrome triple x, 47,xxx and double y syndrome double y, 47, xyy are estimated to affect approximately 1 per 400 births. Testicular size and shape of 47,xyy and 47,xxy men in a. Male infertility related to an aberrant karyotype, 47,xyy. Aula 8 citogenetica e cromossomopatias citogenetica. The y chromosome is one of the sex chromosomes, and the other sex chromosome is called the x chromosome.
There have been several reports of individuals with the 47, xyy chromosome constitution developing acute lymphoblastic leukemia all, acute myeloid leukemia, chronic myelogenous leukemia, or other malignancies. Prevalence of ychromosome sequences and gonadoblastoma in. Patients included 26 boys with 47, xyy, 82 boys with ks, and 50 control boys ages 415 years. A 15yearold patient with a female phenotype visited our hospital owing to a chief complaint of short stature as of the age of 6. The results of our previous pilot study on the frequency of the xyy genotype in prisoners four in 100 and outpatients two in 100 with nca are discussed in relation to the 44% seven in 16 frequency of nca in three series of xyy subjects in whom the presence of nca was sought and. Behavioral and social phenotypes in boys with 47,xyy. Criminality in men with klinefelters syndrome and xyy. The xyy syndrome is an aneuploidy of the sex chromosomes in which a human male receives an extra y chromosome, producing a 47, xyy karyotype.
Unique suggests that parents aim to be patient, calm and firm when dealing with their sons. Despite the fact that 1 in boys 16 have the karyotype 47, xyy xyy, there is a paucity of information about the phenotype, and approximately 85% or more of males with xyy are never diagnosed. Pdf men with 47,xyy syndrome present with varying physical attributes and degrees of infertility. Some males with xyy syndrome will be mosaic, where some of their cells have two y chromosomes and the other cells have the usual one y chromosome. A diagnosis of xyy syndrome is made based upon a thorough clinical evaluation, a detailed patient history, and specialized tests i. Two ova from the mother are fertilized by two sperm from the father. Karyotype analysis 400 belt, g belt showed 47,xyy fig. All structured data from the file and property namespaces is available under the creative commons cc0 license. The person is generally otherwise normal, including normal fertility the condition is generally not inherited from a persons parents but rather occurs as a result of a random event during. Scribd is the worlds largest social reading and publishing site.
Mar 01, 2002 read gastrointestinal stromal tumor in an xyy xy male, cancer genetics and cytogenetics on deepdyve, the largest online rental service for scholarly research with thousands of academic publications available at your fingertips. Objective to investigate the criminal pattern in men between 15 and 70 years of age diagnosed with 47,xxy klinefelters syndrome ks or 47, xyy compared to the general population. Please use one of the following formats to cite this article in your essay, paper or report. The origin of the extra y chromosome in males with a 47,xyy karyotype pdf. Many babies that are born with xyy syndrome do not have any clinical features and symptoms. Desordenes cromosomicos comunes cromosomas 15 y x y y. Xyy syndrome nord national organization for rare disorders. Files are available under licenses specified on their description page. Design registerbased cohort study comparing the incidence of convictions among men with ks and with 47, xyy with age and calendarmatched samples of the general population. In the majority of cases the phenotypic features remain normal.
Get a printable copy pdf file of the complete article 663k, or click on a page image below to browse page by page. Visootsak 2009 found that males with sex chromosomal aneuploidy e. Few patients with xyy syndrome will have infertility. Access to society journal content varies across our titles. Approximately 1 in every males carries an additional y chromosome, either in pure form 47, xyy or in diverse mosaicisms variants. In this study, we report the cases of five unrelated patients with klinefelters syndrome and seizures or eeg epileptiform abnomalities. Atividade analizando cariotipos humanos aberrante 1. The question of causality vs concomitance of nodulocystic acne nca and xyy genotype is examined. If you have access to a journal via a society or association membership, please browse to your society journal, select an article to view, and follow the instructions in this box. Acute lymphoblastic leukemia in a 46,xy47,xyy mosaic male. Enable javascript to view the expandcollapse boxes. Cariotipo euploide eu verdadero, ploide juego a free powerpoint ppt presentation displayed as a flash slide show on id. Xyy syndrome is a genetic condition in which a male has an extra y chromosome.
Most studies about 47, xyy have focused on growth, cognitive development, academic performance, behavioural problems, speech and language skills and neuromuscular status. Most people have two sex chromosomes, with girls having two x chromosomes, and boys having one x and one y chromosome. Although many males with this condition are taller than average, the chromosomal change sometimes causes no unusual physical features. Gastrointestinal stromal tumor in an xyyxy male, cancer. Normalmente varones tienen solamente una copia del cromosoma y y tienen 46 cromosomas total. For language access assistance, contact the ncats public information officer. Mortality among males with 47, xyy is increased due to a host of conditions and diseases. Pdf living with klinefelter syndrome 47,xxy trisomy x. Article pdf available in gene 21 september 20 with 72 reads how we measure reads.
There have been several reports of individuals with the 47,xyy chromosome constitution developing acute lymphoblastic leukemia all, acute myeloid leukemia, chronic myelogenous leukemia, or other malignancies. Men with 47, xyy syndrome present with varying physical attributes and degrees of infertility. The results of our previous pilot study on the frequency of the xyy genotype in prisoners four in 100 and outpatients two in 100 with nca are discussed in relation to the 44% seven in 16. We here report a case of 46,xy 47, xyy syndrome diagnosed in a patient with a female phenotype. Nodulocystic acne as a phenotypic feature of the xyy. These may include being taller than average, acne, and an increased risk of learning problems. Unique, a web site that provides information and support to families affected by rare chromosome disorders, has published several pamphlets about 47, xyy syndrome and behavior disorders. Unfortunately, there is limited current information on how to address behavior issues in a boy with 47, xyy syndrome. Pattern of dna replication of the sex chromosomes in three. Klinefelter syndrome, also known as xxy syndrome, is a condition in boys and men thats caused by an extra x chromosome. They were aged 25 years and followed up both clinically and by means of eeg. Abstract objective to assess the prevalence of ychromosome sequences and gonadoblastoma in patients with turner syndrome ts using molecular techniques. Changes in the cohort composition of turner syndrome and. Abstract 47, xyy karyotype is a y chromosome aneuploidy characterized by an extra copy of the y chromosome in each of the male cells, with an incidence of 1 males.
Testicular size and shape of 47, xyy and 47,xxy men in a doubleblind, doublematched population survey. This chromosomal anomaly occurs in one of 1,000 live male births in the general population, but more frequent in infertile populations. Electroclinical findings in four patients with karyotype. Is microcephaly a sofar unrecognized feature of xyy syndrome. Two of the patients had epilepsy, one had only one isolated generalized tonicclonic seizure, one had febrile. To contrast the behavioral and social phenotypes including a screen for autistic behaviors in boys with 47, xyy syndrome xyy or 47,xxy klinefelter syndrome ks and controls and investigate the effect of prenatal diagnosis on the phenotype. A collection of disease information resources and questions answered by our genetic and rare diseases information specialists for 47, xyy syndrome. A patient with 46,xy47,xyy karyotype and female phenotype. Data source a literature search was performed in pubmed, limiting the period of time to the years 20052014 and using the descriptors. Sindrome 47, xyy genetic and rare diseases information.
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