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Axenfeld-Rieger Syndrome
ISSN: 2165-7386

Journal of Palliative Care & Medicine
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Axenfeld-Rieger Syndrome

Mohamed Abdallahi Ould Hamed*, Abdoulsalam Youssoufou Soulay, Karim Reda and Abdelbarre Oubaaz
Department of Ophthalmology, Med V Military Hospital of Rabat, Morocco
*Corresponding Author: Mohamed Abdallahi Ould Hamed, Department of Ophthalmology, Med V Military Hospital of Rabat, Morocco, Tel: +212655835932, Email: [email protected]

Received: 21-May-2018 / Accepted Date: 24-May-2018 / Published Date: 31-May-2018 DOI: 10.4172/2165-7386.1000336


We report the case of a patient aged 47 who consult for a decrease in visual acuity. Examination of the anterior segment spotting unilateral irrido-trabecular dysgenesis of the right eye with abnormal visibility of the schwalbe line corresponding to a posterior embryotoxon and associated angular abnormalities (Figures 1-3).


Figure 1: Embryotoxon on the temporal side of the right eye.


Figure 2: Embryotoxon on the nasal side of the right eye.


Figure 3: Angular abnormalities of the right eye.

The eye tone measured with Goldmann tonometer showed 14 mmHg in the right eye and 15 mmHg in the left eye. The examination of the fundus of the eye finds symmetrical morphology of the optic discs without pathological excavation.

The remainder of the somatic examination reveals no abnormality associated especially the absence of dental malformation. Chronic glaucoma is seen in 50% of patients [1]. The diagnosis of Axenfeld- Reiger syndrome uncomplicated of chronic glaucoma has been established, despite the absence of signs of Rieger [1]. No treatment has been established. Regular checks have been proposed to detect any complications including glaucoma.


This syndrome is inherited as an autosomal dominant manner. It is found that 2 genes are mainly involved in the transmission; PITX2 gene in 4q25, present in 10-60% of patients, mainly associated with systemic alterations such as dental malformations [2,3].

The other gene responsible is FOXC1 located in 6q25, present in 50% of cases and manifested by ocular alterations, especially glaucoma [2-4]. The differential diagnosis arises with the Peters anomaly which consists of a defect of the posterior surface of the cornea associated with a stromal opacity. Currently, it is suggested that all these abnormalities are actually part of the same syndrome, Axenfeld-Rieger syndrome [5].


Citation: Ould Hamed MA, Soulay AY, Reda K, Oubaaz A (2018) Axenfeld-Rieger Syndrome. J Palliat Care Med 8: 336. DOI: 10.4172/2165-7386.1000336

Copyright: © 2018 Ould Hamed MA, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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