Golestan University of Medical Sciences Repository

Fraser of cryptophthalmosis syndrome: A case report

Khoury, E. and Golalipour, M.-J. and Haidary, K. and Adibi, B. (2004) Fraser of cryptophthalmosis syndrome: A case report. Archives of Iranian Medicine, 7 (4). pp. 307-309. ISSN 10292977 (ISSN)

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Abstract

Fraser or cryptophthalmos syndrome is a rare autosomal recessive disorder characterized by major features such as cryptophthalmos, syndactyly, and abnormal genitalia. Consanguinity is reported in 15-24.8% of the cases. The diagnosis of this syndrome can be made on clinical examination; therefore we present the clinical findings of a rare case of Fraser syndrome in a female infant.

Item Type: Article
Additional Information: Unmapped bibliographic data: LA - English [Field not mapped to EPrints] J2 - Arch. Iran. Med. [Field not mapped to EPrints] AD - Department of Obstetrics, Golestan Univ. of Medical Sciences, P.O. Box 49165-568, Gorgan, Iran [Field not mapped to EPrints] AD - Department of Embryology/Histology, Golestan Univ. of Medical Sciences, P.O. Box 49165-568, Gorgan, Iran [Field not mapped to EPrints] AD - Department of Ophthalmology, Golestan Univ. of Medical Sciences, P.O. Box 49165-568, Gorgan, Iran [Field not mapped to EPrints] DB - Scopus [Field not mapped to EPrints]
Uncontrolled Keywords: Cryptophthalmos syndrome, Cryptophthalmos-syndactyly syndrome, Fraser syndrome, article, brachydactyly, case report, clinical examination, clinical feature, coloboma, consanguinity, cornea opacity, ear malformation, eyebrow, eyelash, female, Fraser syndrome, genital malformation, hair growth, human, infant, keratitis, microphthalmia, nose malformation, palpebral fissure anomaly, surgical technique, syndactyly, upper eyelid, visual system examination
Subjects: مقالات نمایه شده محققین دانشگاه در سایت ,Web of Science ,Scopus
Divisions: معاونت تحقیقات و فناوری
Depositing User: GOUMS
Date Deposited: 15 Apr 2015 09:00
Last Modified: 04 Feb 2017 09:54
URI: http://eprints.goums.ac.ir/id/eprint/2468

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