Abstract
Fraser syndrome (FS) is a rare disorder characterized by a combination of acrofacial and urogenital malformations with or without cryptophthalmos. We report a newborn and its two elder siblings who had multiple congenital anomalies and clinico-radiological features consistent with FS.
Keywords
Publication details
- DOI
- 10.4103/0974-620x.83661
- Journal
- Oman Journal of Ophthalmology, 4(2), 87-89
- Publisher
- Medknow Publications
- Open access
- Gold open access
Cite this article
APA 7
Kalaniti, K., & Sandhya, V. (2011). Fraser syndrome in three consecutive siblings. Oman Journal of Ophthalmology, 4(2), 87-89. https://doi.org/10.4103/0974-620x.83661
MLA 9
Kalaniti, Kaarthigeyan, and V Sandhya. "Fraser syndrome in three consecutive siblings." Oman Journal of Ophthalmology, vol. 4, no. 2, 2011, pp. 87-89. https://doi.org/10.4103/0974-620x.83661.
Chicago (author–date)
Kalaniti, Kaarthigeyan, and V Sandhya. 2011. "Fraser syndrome in three consecutive siblings." Oman Journal of Ophthalmology 4 (2): 87-89. https://doi.org/10.4103/0974-620x.83661.
Harvard
Kalaniti, K. and Sandhya, V. (2011) 'Fraser syndrome in three consecutive siblings', Oman Journal of Ophthalmology, 4(2), pp. 87-89. doi:10.4103/0974-620x.83661.
Vancouver
Kalaniti K, Sandhya V. Fraser syndrome in three consecutive siblings. Oman Journal of Ophthalmology. 2011;4(2):87-89. doi:10.4103/0974-620x.83661
IEEE
K. Kalaniti, and V. Sandhya, "Fraser syndrome in three consecutive siblings," Oman Journal of Ophthalmology, vol. 4, no. 2, pp. 87-89, 2011, doi: 10.4103/0974-620x.83661.