Trochlear nerve agenesis in a patient with 18q22.2q23 deletion.

Yang, Hee Kyung; Kim, Hwa Young; Kim, Jae Hyoung; Hwang, Jeong-Min

Yang, Hee Kyung; Kim, Hwa Young; Kim, Jae Hyoung; Hwang, Jeong-Min.

Afiliação

Yang HK; Department of Ophthalmology, Seoul National University College of Medicine, Seoul National University Bundang Hospital, 82, Gumi-Ro 173 Beon-Gil, Bundang-Gu, Seongnam-Si, 13620, Gyeonggi-Do, Korea.
Kim HY; Department of Pediatrics, Seoul National University College of Medicine, Seoul National University Bundang Hospital, 82, Gumi-Ro 173 Beon-Gil, Bundang-Gu, Seongnam-Si, 13620, Gyeonggi-Do, Korea.
Kim JH; Department of Radiology, Seoul National University College of Medicine, Seoul National University Bundang Hospital, 82, Gumi-Ro 173 Beon-Gil, Bundang-Gu, Seongnam-Si, 13620, Gyeonggi-Do, Korea. jaehkim@snu.ac.kr.
Hwang JM; Department of Ophthalmology, Seoul National University College of Medicine, Seoul National University Bundang Hospital, 82, Gumi-Ro 173 Beon-Gil, Bundang-Gu, Seongnam-Si, 13620, Gyeonggi-Do, Korea. hjm@snubh.org.

Neurol Sci ; 45(8): 4083-4085, 2024 Aug.

Article em En | MEDLINE | ID: mdl-38691274

Assuntos

Deleção Cromossômica; Cromossomos Humanos Par 18; Humanos; Cromossomos Humanos Par 18/genética; Masculino; Nervo Troclear/anormalidades; Feminino; Doenças do Nervo Troclear/genética; Doenças do Nervo Troclear/diagnóstico

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 18 / Deleção Cromossômica Limite: Female / Humans / Male Idioma: En Ano de publicação: 2024 Tipo de documento: Article

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