Authors
- Hamdan H. Al-Hazmi, The Montreal Children's Hospital, C529, 2300, rue Tupper, Montreal, Quebec H3H 1P3, Canada. Tel. +1 (514) 412 4366. Fax. +1 (514) 412 4384. E-mail: drhamdanhh{at}hotmail.com
- Ayman A. Hammad, The Montreal Children's Hospital, C529, 2300, rue Tupper, Montreal, Quebec H3H 1P3, Canada. Tel. +1 (514) 412 4366. Fax. +1 (514) 412 4384. E-mail: drhamdanhh{at}hotmail.com
- Roman Jednak, The Montreal Children's Hospital, C529, 2300, rue Tupper, Montreal, Quebec H3H 1P3, Canada. Tel. +1 (514) 412 4366. Fax. +1 (514) 412 4384. E-mail: drhamdanhh{at}hotmail.com
- Mohamed T. El-Sherbiny, The Montreal Children's Hospital, C529, 2300, rue Tupper, Montreal, Quebec H3H 1P3, Canada. Tel. +1 (514) 412 4366. Fax. +1 (514) 412 4384. E-mail: drhamdanhh{at}hotmail.com
Abstract
The urofacial or Ochoa syndrome is a rare disease. We report on 2 patients of middle-eastern origin, with a review of the current literature to further document the existence of this syndrome, and to increase the general awareness of the classical facial characteristics, which facilitates diagnosis.
Recommended Citation
Al-Hazmi, Hamdan H.; Hammad, Ayman A.; Jednak, Roman; and El-Sherbiny, Mohamed T.
(2007)
"Urofacial syndrome,"
Saudi Medical Journal: Vol. 28:
Iss.
12, Article 23.
DOI: https://doi.org/10.15537/1658-3175.4170
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