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. Keywords: Atypical Coats' Syndrome, Exudative retinopathy with telangiectasia, Facioscapulohumeral dystroph
Purpose: To describe a case of Coats Plus Syndrome (CPS), a vision and life threatening disease belo...
Background: Facioscapulohumeral dystrophy (FSHD) is a rare hereditary disease with a prevalence of 2...
Background: Facioscapulohumeral dystrophy (FSHD) is a rare hereditary disease with a prevalence of 2...
Purpose: To report a unique case of atypical Coats' Syndrome in an 80 year old female with facioscap...
International audienceOBJECTIVE: To investigate the frequency of Coats syndrome and its association ...
Coats' disease is a nonhereditary ocular disease, with no systemic manifestation, first described by...
Purpose: To evaluate the rarity, clinical features and management of Coats disease characterized by ...
Investigators at University of Rochester Medical Center, NY; Hopital Archet-CHU de Nice, France; and...
The retinal telangiectasias (idiopathic juxtafoveal telangiectasis, Leber’s miliary aneurysms and Co...
Coats disease is a congenital retinal vascular disease, which is seen commonly in childhood and remi...
Introduction: Duane retraction syndrome and Coats' disease are two relatively rare ocular conditions...
Purpose: The aim of this report was to demonstrate a case of Coats disease in a patient with concurr...
Coats' disease is an idiopathic, primary vascular anomaly of the retina often presenting with retina...
International audienceObjective To determine whether the clinical presentation of Coats disease diff...
A forty-four-year-old female patient known for FSHD type I, with unremarkable past ocular history, c...
Purpose: To describe a case of Coats Plus Syndrome (CPS), a vision and life threatening disease belo...
Background: Facioscapulohumeral dystrophy (FSHD) is a rare hereditary disease with a prevalence of 2...
Background: Facioscapulohumeral dystrophy (FSHD) is a rare hereditary disease with a prevalence of 2...
Purpose: To report a unique case of atypical Coats' Syndrome in an 80 year old female with facioscap...
International audienceOBJECTIVE: To investigate the frequency of Coats syndrome and its association ...
Coats' disease is a nonhereditary ocular disease, with no systemic manifestation, first described by...
Purpose: To evaluate the rarity, clinical features and management of Coats disease characterized by ...
Investigators at University of Rochester Medical Center, NY; Hopital Archet-CHU de Nice, France; and...
The retinal telangiectasias (idiopathic juxtafoveal telangiectasis, Leber’s miliary aneurysms and Co...
Coats disease is a congenital retinal vascular disease, which is seen commonly in childhood and remi...
Introduction: Duane retraction syndrome and Coats' disease are two relatively rare ocular conditions...
Purpose: The aim of this report was to demonstrate a case of Coats disease in a patient with concurr...
Coats' disease is an idiopathic, primary vascular anomaly of the retina often presenting with retina...
International audienceObjective To determine whether the clinical presentation of Coats disease diff...
A forty-four-year-old female patient known for FSHD type I, with unremarkable past ocular history, c...
Purpose: To describe a case of Coats Plus Syndrome (CPS), a vision and life threatening disease belo...
Background: Facioscapulohumeral dystrophy (FSHD) is a rare hereditary disease with a prevalence of 2...
Background: Facioscapulohumeral dystrophy (FSHD) is a rare hereditary disease with a prevalence of 2...