Autism spectrum disorder in a patient with Nicolaides-Baraitser Syndrome: case report

被引:0
|
作者
Lopes, Derek Chaves [1 ,3 ]
Mendes, Lorenna Sena Teixeira [2 ]
Ferreira, Ines Catao Henriques [2 ]
机构
[1] Escola Super Ciencias Saude, Brasilia, DF, Brazil
[2] Fundacao Ensino & Pesquisa Ciencias Saude, Child & Adolescent Psychiat Residency Program, Brasilia, DF, Brazil
[3] SMHN Quadra 03,Room A,Bldg 1,Edificio Fepecs, BR-70710907 Brasilia, DF, Brazil
来源
EINSTEIN-SAO PAULO | 2023年 / 21卷
关键词
Autism spectrum disorder; Nicolaides Baraitser syndrome; Neurodevelopmental Disorders; Brazil;
D O I
10.31744/einstein_journal/2023RC0480
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Nicolaides-Baraitser Syndrome is a rare genetic condition that clinically presents with intellectual disabilities, facial and bone changes, and sparse hair. In Brazil, only one case has been previously reported without genetic confirmation. We present the case of an 8-year-old boy, clinically and genetically diagnosed with Nicolaides-Baraitser Syndrome, who developed autism spectrum disorder characteristics with a formal diagnosis at the age of eight. Diagnosing autism spectrum disorder in patients with intellectual disabilities is a clinical challenge requiring careful evaluation.
引用
收藏
页码:1 / 3
页数:3
相关论文
共 50 条
  • [41] Autism Spectrum Disorder and Suicide: A Case Report
    Fatani, Abrar N.
    Alasiri, Nouf M.
    Gasem, Osama A.
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2024, 16 (07)
  • [42] Food intake restriction in patient with autism spectrum disorder and Moebius syndrome, a strong association. A case report
    Del Sol Calderon, P.
    Izquierdo de la Puente, A.
    Fernandez, R.
    Garcia Moreno, M.
    Erdocia, A.
    EUROPEAN PSYCHIATRY, 2024, 67 : S454 - S454
  • [43] Autism spectrum disorder and Coffin-Siris syndrome-Case report
    Milutinovic, Luka
    Grujicic, Roberto
    Mandic Maravic, Vanja
    Joksic, Ivana
    Ljubomirovic, Natasa
    Milovancevic, Milica Pejovic
    FRONTIERS IN PSYCHIATRY, 2023, 14
  • [44] Cri du Chat Syndrome Coexistent with Autism Spectrum Disorder: A Case Report
    Firat, Sumeyra
    Senor, Pinar Uran
    Aysev, Fatma Ayla Soykan
    PSYCHIATRY AND BEHAVIORAL SCIENCES, 2018, 8 (02): : 89 - 92
  • [45] Williams Syndrome Associated With Autism Spectrum Disorder: Case Report and Review of the Literature
    Carvalho, Max M.
    Mazza, Jeanne
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2020, 12 (08)
  • [46] A CASE REPORT OF A CAT-EYE SYNDROME PRESENTING WITH AN AUTISM SPECTRUM DISORDER
    Barbosa, Sofia
    Lages, Marta
    Borja-Santos, Nuno
    Goncalves, Patricia
    Barreta, Ana
    Maia, Teresa
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2019, 29 : 1337 - 1338
  • [47] Living birth following preimplantation genetic testing for monogenic disorders to prevent low-level germline mosaicism related Nicolaides-Baraitser syndrome
    Pan, Jiexue
    Li, Jie
    Chen, Songchang
    Xu, Chenming
    Huang, Hefeng
    Jin, Li
    FRONTIERS IN GENETICS, 2022, 13
  • [48] Report of a Patient With Temple-Baraitser Syndrome
    Yesil, Gozde
    Guler, Serhat
    Yuksel, Adnan
    Alanay, Yasemin
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2014, 164 (03) : 848 - 851
  • [49] Cooccurrence of Two Different Genetic Diseases: A Case of Valproic Acid Hepatotoxicity in Nicolaides-Baraitser Syndrome ( SMARCA2 Mutation)-Due to a POLG1 -Related Effect?
    Hofmeister, Benedikt
    von Stuelpnagel, Celina
    Berweck, Steffen
    Abicht, Angela
    Kluger, Gerhard
    Weber, Peter
    NEUROPEDIATRICS, 2020, 51 (01) : 49 - 52
  • [50] De novo SMARCA2 variants clustered outside the helicase domain cause a new recognizable syndrome with intellectual disability and blepharophimosis distinct from Nicolaides-Baraitser syndrome
    Cappuccio, Gerarda
    Sayou, Camille
    Le Tanno, Pauline
    Tisserant, Emilie
    Bruel, Ange-Line
    El Kennani, Sara
    Sa, Joaquim
    Low, Karen J.
    Dias, Cristina
    Havlovicova, Marketa
    Hancarova, Miroslava
    Eichler, Evan E.
    Devillard, Francoise
    Moutton, Sebastien
    Van-Gils, Julien
    Dubourg, Christele
    Odent, Sylvie
    Gerard, Benedicte
    Piton, Amelie
    Yamamoto, Toshiyuki
    Okamoto, Nobuhiko
    Firth, Helen
    Metcalfe, Kay
    Moh, Anna
    Chapman, Kimberly A.
    Aref-Eshghi, Erfan
    Kerkhof, Jennifer
    Torella, Annalaura
    Nigro, Vincenzo
    Perrin, Laurence
    Piard, Juliette
    Le Guyader, Gwenael
    Jouan, Thibaud
    Thauvin-Robinet, Christel
    Duffourd, Yannis C.
    George-Abraham, Jaya K.
    Buchanan, Catherine A.
    Williams, Denise
    Kini, Usha
    Wilson, Kate
    Sousa, Sergio B.
    Hennekam, Raoul C. M.
    Sadikovic, Bekim
    Thevenon, Julien
    Govin, Jerome
    Vitobello, Antonio
    Brunetti-Pierri, Nicola
    Casari, Giorgio
    Pinelli, Michele
    Musacchia, Francesco
    GENETICS IN MEDICINE, 2020, 22 (11) : 1838 - 1850