Published In
The Eurasian Journal of Medicine
Volume 37 · Issue 1 · January 2005
Pages: 19-21
History
Published Online: September 3, 2019
Copyright © 2005 The Eurasian Journal of Medicine
Abdulgani Tatar
Department of Medical Genetics (AT
Rahmi Örs
Department of Medical Genetics (AT
Sıtkı Öztaş
Department of Medical Genetics (AT
Tatar, A., Örs, R., & Öztaş, S. (2019). A CASE WITH FRYNS SYNDROME-LIKE PHENOTYPE. The Eurasian Journal of Medicine, 37(1), 19–21. Retrieved from https://www.eajm.org/index.php/pub/article/view/2153
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Abstract
Abstract
Fryns syndrome is a rare autosomal recessive disorder with a heterogeneous phenotype. So far, about 112 cases have been reported and phenotypic heterogeneity has been shown. We are describing a male patient having facial dysmorphism, radial polydactyly, nail hypoplasia, ventricular septal defect, patent ductus arteriosus and intestinal adhesions. The patient was born after in vitro fertilization. With these findings, we thought that the patient may be a case with Fryns syndrome-like phenotype.
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Article Info
Published In
Journal
The Eurasian Journal of Medicine
Volume / Issue
Volume 37 · Issue 1 · January 2005
Pages
19-21
History
Published Online
September 3, 2019
Copyright
Copyright (c) 2005 The Eurasian Journal of Medicine
Affiliations
Abdulgani Tatar
Department of Medical Genetics (AT
Rahmi Örs
Department of Medical Genetics (AT
Sıtkı Öztaş
Department of Medical Genetics (AT
Cite this Article
Tatar, A., Örs, R., & Öztaş, S. (2019). A CASE WITH FRYNS SYNDROME-LIKE PHENOTYPE. The Eurasian Journal of Medicine, 37(1), 19–21. Retrieved from https://www.eajm.org/index.php/pub/article/view/2153
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