Purpose: To report a unique case of atypical Coats' Syndrome in an 80 year old female with facioscapulohumeral dystrophy. Observations: An 80 years old female was diagnosed clinically of retinal telangiectasia with exudation threatening the fovia. She received a successful macular laser photocoagulation with subsequent cessation of leakage. Conclusions and importance: This case is in keeping with Coats' syndrome in fascioscapulohumeral dystrophy, which classically affects young male subjects - making this patient an obvious outlier. This once again reflects the variation in phenotypic manifestations of inherited disorders
Purpose. We describe an atypical case of a patient with Coats disease that re-emerged after 30 years...
Background: Facioscapulohumeral dystrophy (FSHD) is a rare hereditary disease with a prevalence of 2...
Purpose: The aim of this report was to demonstrate a case of Coats disease in a patient with concurr...
Purpose: To report a unique case of atypical Coats' Syndrome in an 80 year old female with facioscap...
Coats' disease is a nonhereditary ocular disease, with no systemic manifestation, first described by...
Investigators at University of Rochester Medical Center, NY; Hopital Archet-CHU de Nice, France; and...
International audienceOBJECTIVE: To investigate the frequency of Coats syndrome and its association ...
Coats disease is a congenital retinal vascular disease, which is seen commonly in childhood and remi...
Purpose: To evaluate the rarity, clinical features and management of Coats disease characterized by ...
A forty-four-year-old female patient known for FSHD type I, with unremarkable past ocular history, c...
International audienceObjective To determine whether the clinical presentation of Coats disease diff...
The retinal telangiectasias (idiopathic juxtafoveal telangiectasis, Leber’s miliary aneurysms and Co...
Introduction: Duane retraction syndrome and Coats' disease are two relatively rare ocular conditions...
Background: Facioscapulohumeral dystrophy (FSHD) is a rare hereditary disease with a prevalence of 2...
Coats' disease is an idiopathic, primary vascular anomaly of the retina often presenting with retina...
Purpose. We describe an atypical case of a patient with Coats disease that re-emerged after 30 years...
Background: Facioscapulohumeral dystrophy (FSHD) is a rare hereditary disease with a prevalence of 2...
Purpose: The aim of this report was to demonstrate a case of Coats disease in a patient with concurr...
Purpose: To report a unique case of atypical Coats' Syndrome in an 80 year old female with facioscap...
Coats' disease is a nonhereditary ocular disease, with no systemic manifestation, first described by...
Investigators at University of Rochester Medical Center, NY; Hopital Archet-CHU de Nice, France; and...
International audienceOBJECTIVE: To investigate the frequency of Coats syndrome and its association ...
Coats disease is a congenital retinal vascular disease, which is seen commonly in childhood and remi...
Purpose: To evaluate the rarity, clinical features and management of Coats disease characterized by ...
A forty-four-year-old female patient known for FSHD type I, with unremarkable past ocular history, c...
International audienceObjective To determine whether the clinical presentation of Coats disease diff...
The retinal telangiectasias (idiopathic juxtafoveal telangiectasis, Leber’s miliary aneurysms and Co...
Introduction: Duane retraction syndrome and Coats' disease are two relatively rare ocular conditions...
Background: Facioscapulohumeral dystrophy (FSHD) is a rare hereditary disease with a prevalence of 2...
Coats' disease is an idiopathic, primary vascular anomaly of the retina often presenting with retina...
Purpose. We describe an atypical case of a patient with Coats disease that re-emerged after 30 years...
Background: Facioscapulohumeral dystrophy (FSHD) is a rare hereditary disease with a prevalence of 2...
Purpose: The aim of this report was to demonstrate a case of Coats disease in a patient with concurr...