Oculocutaneous Albinism and Autism: A Case Report and Review of Literature

被引:7
|
作者
Hesapcioglu, Selma Tural [1 ]
机构
[1] Karadeniz Tech Univ, Fac Med, Trazon, Turkey
关键词
Autism; child; oculocutaneous albinism;
D O I
10.5350/DAJPN2013260213
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Autistic disorder is a highly heritable disorder characterized by impaired communication, social interaction, and repetitive behaviors. Several inherited medical and psychological disorders have been reported in association with childhood autism and many of these disorders shed light on the role of genetics in the etiology of childhood autism. Association of autism and oculocutaneous albinism is rarely reported in the literature. Herein, we report the joint occurrence of autistic disorder (AD) and oculocutaneous albinism (OCA) in a two-year and six-month old boy. This association was documented in a few previous reports about the affected individuals and families of individuals with childhood autism. All these reports and this case connote whether childhood autism has any genetic and clinical relationship with oculocutaneous albinism.
引用
收藏
页码:215 / 218
页数:4
相关论文
共 50 条
  • [31] Dermoscopy of Amelanotic Melanoma in a Patient With Oculocutaneous Albinism
    Uyar, Belkis
    Elmas, Omer Faruk
    Kilitci, Asuman
    Tad, Murat
    DERMATOLOGY PRACTICAL & CONCEPTUAL, 2020, 10 (03):
  • [32] Sociodemographic and visual characteristics of individuals with oculocutaneous albinism in Botswana
    Panicker, Thanuja
    Madheswaran, Gopinath
    AFRICAN VISION AND EYE HEALTH JOURNAL, 2025, 84 (01):
  • [33] Genetic Variability in Slovenian Cohort of Patients with Oculocutaneous Albinism
    Hovnik, Tinka
    Debeljak, Marusa
    Pompe, Manca Tekavcic
    Bertok, Sara
    Battelino, Tadej
    Kranjc, Branka Stirn
    Podkrajsek, Katarina Trebusak
    ACTA CHIMICA SLOVENICA, 2021, 68 (03) : 683 - 692
  • [34] Phacoemulsification and intraocular lens implantation in patients with oculocutaneous albinism
    Davila, Pedro J.
    Ulloa-Padilla, Jan P.
    Izquierdo, Natalio J.
    OPHTHALMIC GENETICS, 2017, 38 (02) : 157 - 160
  • [35] Foveal thickness and macular volume in patients with oculocutaneous albinism
    Izquierdo, Natalio J.
    Emanuelli, Andres
    Izquierdo, Juan C.
    Garcia, Maribel
    Cadilla, Carmen
    Berrocal, Maria H.
    RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, 2007, 27 (09): : 1227 - 1230
  • [36] Visual function and visual ability in adolescents with oculocutaneous albinism
    Naipal, Shivani
    Rampersad, Nishanee
    BRITISH JOURNAL OF VISUAL IMPAIRMENT, 2022, 40 (02) : 327 - 334
  • [37] Genetic analyses of Chinese patients with digenic oculocutaneous albinism
    Wei Ai-hua
    Yang Xiu-min
    Lian Shi
    Li Wei
    CHINESE MEDICAL JOURNAL, 2013, 126 (02) : 226 - 230
  • [38] A case report and literature review of autism and attention deficit hyperactivity disorder in paediatric chronic pain
    Lipsker, Camilla Wiwe
    von Heijne, Margareta
    Bolte, Sven
    Wicksell, Rikard K.
    ACTA PAEDIATRICA, 2018, 107 (05) : 753 - 758
  • [39] Oculocutaneous albinism type 1: The last 100 years
    Oetting, WS
    Fryer, JP
    Shriram, S
    King, RA
    PIGMENT CELL RESEARCH, 2003, 16 (03): : 307 - 311
  • [40] FOVEAL HYPOPLASIA IN COMPLETE OCULOCUTANEOUS ALBINISM - A HISTOPATHOLOGIC STUDY
    MIETZ, H
    GREEN, WR
    WOLFF, SM
    ABUNDO, GP
    RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, 1992, 12 (03): : 254 - 260