<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.4 20241031//EN"
        "https://jats.nlm.nih.gov/publishing/1.4/JATS-journalpublishing1-4.dtd">
<article  article-type="case-report"        dtd-version="1.4">
            <front>

                <journal-meta>
                                                                <journal-id>uludağ tıp derg</journal-id>
            <journal-title-group>
                                                                                    <journal-title>Journal of Uludağ University Medical Faculty</journal-title>
            </journal-title-group>
                            <issn pub-type="ppub">1300-414X</issn>
                                        <issn pub-type="epub">2645-9027</issn>
                                                                                            <publisher>
                    <publisher-name>Bursa Uludağ Üniversitesi</publisher-name>
                </publisher>
                    </journal-meta>
                <article-meta>
                                        <article-id pub-id-type="doi">10.32708/uutfd.1478893</article-id>
                                                                <article-categories>
                                            <subj-group  xml:lang="en">
                                                            <subject>Psychiatry</subject>
                                                    </subj-group>
                                            <subj-group  xml:lang="tr">
                                                            <subject>Psikiyatri</subject>
                                                    </subj-group>
                                    </article-categories>
                                                                                                                                                        <title-group>
                                                                                                                        <trans-title-group xml:lang="tr">
                                    <trans-title>Şizofreni ile Birliktelik Gösteren Capgras Sendromu: Bir Ergen Olgu Sunumu</trans-title>
                                </trans-title-group>
                                                                                                                                                                                                <article-title>Capgras Syndrome Accompanying Schizophrenia: An Adolescent Case Report</article-title>
                                                                                                    </title-group>
            
                                                    <contrib-group content-type="authors">
                                                                        <contrib contrib-type="author">
                                                                    <contrib-id contrib-id-type="orcid">
                                        https://orcid.org/0000-0002-5879-9412</contrib-id>
                                                                <name>
                                    <surname>Eroğlu</surname>
                                    <given-names>Mehtap</given-names>
                                </name>
                                                                    <aff>Ankara Bilkent City Hospital, Child and Adolescent Mental Health and Diseases Clinic Ankara, Türkiye.</aff>
                                                            </contrib>
                                                                                </contrib-group>
                        
                                        <pub-date pub-type="pub" iso-8601-date="20241008">
                    <day>10</day>
                    <month>08</month>
                    <year>2024</year>
                </pub-date>
                                        <volume>50</volume>
                                        <issue>2</issue>
                                        <fpage>313</fpage>
                                        <lpage>315</lpage>
                        
                        <history>
                                    <date date-type="received" iso-8601-date="20240505">
                        <day>05</day>
                        <month>05</month>
                        <year>2024</year>
                    </date>
                                                    <date date-type="accepted" iso-8601-date="20240725">
                        <day>07</day>
                        <month>25</month>
                        <year>2024</year>
                    </date>
                            </history>
                                        <permissions>
                    <copyright-statement>Copyright © 1975, Uludağ Üniversitesi Tıp Fakültesi Dergisi</copyright-statement>
                    <copyright-year>1975</copyright-year>
                    <copyright-holder>Uludağ Üniversitesi Tıp Fakültesi Dergisi</copyright-holder>
                </permissions>
            
                                                                                                <trans-abstract xml:lang="tr">
                            <p>Capgras sendromunda (CS), hasta orijinal kişi ya da nesnelerin tıpatıp benzerleri (sahteleri) ile yer değiştirdiğine inanır. Sendrom nadiren saf haliyle ortaya çıkar. Genellikle psikotik hastalık ve organik patolojiye eşlik eder. Capgras sendromu bütün yaş gruplarında ortaya çıkabilir ve kadınlarda görülme sıklığı daha fazladır. Bu yazıda saldırganlık, çevresine zarar verme ve DNA testi yaptırmak isteme şikayetiyle hastaneye başvuran 16 yaşında kadın hasta olgusu sunulacaktır. İlk başvuru muayenesinde Capgras sanrılarının olduğu görülmüş olup psikiyatri kliniğinde yatırılarak takip edilmiştir. Erken başlangıçlı psikotik bozukluk tanısıyla izlenen hastanın takiplerde erken başlangıçlı Şizofreni ile birliktelik gösteren CS olgusu olduğu belirlenmiştir. Erken başlangıçlı Şizofreni nadir görülen bir durumdur ve CS&#039;nin bu yaşta başlaması da nadirdir. Olgumuz nadir görülen bir durum olan CS&#039;nin ergenlik döneminde de görülebileceğini göstermesi açısından değerlidir.</p></trans-abstract>
                                                                                                                                    <abstract><p>In Capgras syndrome, the patient believes that the original person or objects have been replaced by identical ones (fakes). The syndrome rarely occurs in its pure form. It often accompanies psychotic illness and organic pathology. Capgras syndrome can occur in all age groups and is more common in women. In this article, the case of a 16-year-old female patient who applied to the hospital with complaints of aggression, harming her environment and wanting to have a DNA test will be presented. During her first admission examination, she was found to have Capgras delusions, and she was hospitalized and monitored in a psychiatric clinic. The patient, who was followed up with a diagnosis of early-onset psychotic disorder, was determined to be a case of CS accompanying Schizophrenia. Early-onset Schizophrenia is already a rare condition, and the onset of CS at this age is uncommon. Our case is valuable as it shows that CS, a rare condition, can also be seen in adolescence.</p></abstract>
                                                            
            
                                                                                        <kwd-group>
                                                    <kwd>adolescent</kwd>
                                                    <kwd>  capgras</kwd>
                                                    <kwd>  schizophrenia</kwd>
                                            </kwd-group>
                            
                                                <kwd-group xml:lang="tr">
                                                    <kwd>ergen</kwd>
                                                    <kwd>  capgras</kwd>
                                                    <kwd>  şizofreni</kwd>
                                            </kwd-group>
                                                                                                                                        </article-meta>
    </front>
    <back>
                            <ref-list>
                                    <ref id="ref1">
                        <label>1</label>
                        <mixed-citation publication-type="journal">1. Cipriani G, Vedovello M, Ulivi M, Lucetti C, Di Fiorino A,Nuti A. Delusional misidentification syndromes and dementia:a border zone between neurology and psychiatry. American Journal of Alzheimer&#039;s Disease &amp; Other Dementias®.2013;28(7):671-78.</mixed-citation>
                    </ref>
                                    <ref id="ref2">
                        <label>2</label>
                        <mixed-citation publication-type="journal">2. Edelstyn NM, Oyebode F, Barrett K. The delusions of Capgrasand intermetamorphosis in a patient with right-hemisphere white-matter pathology. Psychopathology. 2001;34(6):299-304.</mixed-citation>
                    </ref>
                                    <ref id="ref3">
                        <label>3</label>
                        <mixed-citation publication-type="journal">3. Salvatore P, Bhuvaneswar C, Tohen M, Khalsa H-MK, Maggini C, Baldessarini RJ. Capgras&#039; syndrome in first-episode psychotic disorders. Psychopathology. 2014;47(4):261-69.</mixed-citation>
                    </ref>
                                    <ref id="ref4">
                        <label>4</label>
                        <mixed-citation publication-type="journal">4. Gibson R, Lowe G, Morgan K, Henry M, De La Haye W, IronsA.Capgras syndrome presenting in an adolescent girl in theCaribbean. West Indian Medical Journal. 2013;62(1).</mixed-citation>
                    </ref>
                                    <ref id="ref5">
                        <label>5</label>
                        <mixed-citation publication-type="journal">5. Breitborde NJ, Srihari VH, Woods SW. Review of theoperational definition for first‐episode psychosis. Early intervention in psychiatry. 2009;3(4):259-65.</mixed-citation>
                    </ref>
                                    <ref id="ref6">
                        <label>6</label>
                        <mixed-citation publication-type="journal">6. Association AP. Diagnostic and statistical manual of mentaldisorders. Text revision. 2000.</mixed-citation>
                    </ref>
                                    <ref id="ref7">
                        <label>7</label>
                        <mixed-citation publication-type="journal">7. Förstl H, Almeida OP, Owen AM, Burns A, Howard R.Psychiatric, neurological and medical aspects ofmisidentification syndromes: a review of 260 cases.Psychological medicine. 1991;21(4):905-10.</mixed-citation>
                    </ref>
                                    <ref id="ref8">
                        <label>8</label>
                        <mixed-citation publication-type="journal">8. Devinsky O. Delusional misidentifications and duplications: right brain lesions, left brain delusions. Neurology. 2009;72(1):80-87.</mixed-citation>
                    </ref>
                                    <ref id="ref9">
                        <label>9</label>
                        <mixed-citation publication-type="journal">9. Christodoulou GN. The delusional misidentificationsyndromes. Bibl Psychiatr. 1986.</mixed-citation>
                    </ref>
                                    <ref id="ref10">
                        <label>10</label>
                        <mixed-citation publication-type="journal">10. Enoch D, Puri BK, Ball H. Uncommon psychiatric syndromes. Routledge; 2020.</mixed-citation>
                    </ref>
                            </ref-list>
                    </back>
    </article>
