New Ocular Associations in Sanjad-Sakati Syndrome: Case report from Oman.

Haider, Agha S; Ganesh, Anuradha; Al-Kindi, Adila; Al-Hinai, Ahmad; Al-Kharousi, Nadia; Al-Yaroubi, Saif; Al-Zuhaibi, Sana

Haider, Agha S; Ganesh, Anuradha; Al-Kindi, Adila; Al-Hinai, Ahmad; Al-Kharousi, Nadia; Al-Yaroubi, Saif; Al-Zuhaibi, Sana.

Afiliação

Haider AS; Departments of Ophthalmology, Sultan Qaboos University Hospital, Muscat, Oman.
Ganesh A; Departments of Ophthalmology, Sultan Qaboos University Hospital, Muscat, Oman.
Al-Kindi A; Genetics, Sultan Qaboos University Hospital, Muscat, Oman.
Al-Hinai A; Departments of Ophthalmology, Sultan Qaboos University Hospital, Muscat, Oman.
Al-Kharousi N; Departments of Ophthalmology, Sultan Qaboos University Hospital, Muscat, Oman.
Al-Yaroubi S; Child Health, Sultan Qaboos University Hospital, Muscat, Oman.
Al-Zuhaibi S; Departments of Ophthalmology, Sultan Qaboos University Hospital, Muscat, Oman.

Sultan Qaboos Univ Med J ; 14(3): e401-4, 2014 Aug.

Article em En | MEDLINE | ID: mdl-25097779

Palavras-chave

Case Report; Corneal Opacity, congenital; Hypoparathyroidism; Nanophthalmos; Oman; Persistent Fetal Vasculature Syndrome; Sanjad-Sakati Syndrome; TBCE Protein, human

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Sultan Qaboos Univ Med J Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Omã

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