Ectodermal Dysplasia is a disorder that occurs due to abnormal development of at least two major ectodermal derivatives in the developing embryo. Author report the case of a 10 year old male child who was referred to our department with complaints of absent sweating, foreign body sensation and watering in both eyes for past few months. The family history could be traced to four generations and there was an observed trend of increase in severity of signs and symptoms occurring at younger age. The purpose of this case report is to create awareness in the Ophthalmic community about the diagnosis and clinical manifestations of the disorder. This case highlights the role of multidisciplinary approach for management of systemic disease, genetic ...
Purpose: To report a case of advanced childhood glaucoma secondary to congenital ectropion uveae (CE...
We report four cases of ectodermal dysplasia. Three of them are hypohidrotic ectodermal dysplasia (H...
The hypohidrotic ectodermal dysplasia (HED) is a rare genetic disease characterized by the absence o...
Hypohidrotic ectodermal dysplasia (HED), also known as Christ-Siemens-Touraine syndrome, is a rare X...
Ectodermal dysplasia is a hereditary disorder that occurs as a consequence of disturbances in the ec...
ABSTRACT Background and Setting: Hypohidrotic (anhidrotic) ectodermal dysplasia (HED) is a congenita...
Ectodermal dysplasia (ED) is a rare heterogenous group of ectodermal disorder, which primarily affec...
Ectodermal dysplasia is a hereditary disease characterized by a congenital dysplasia of one or more ...
Ichthyosiform dermatoses are a group of hereditary disorders characterized by dryness and roughness ...
Ectodermal dysplasia (ED) is a inherited genetic disorder with manifestations of abnormalities in mo...
Ectodermal dysplasia is a hereditary disorder that occurs as a consequence of disturbances in the ec...
Ectodermal dysplasia (ED) is a rare hereditary disorder involving two or more of the ectodermal stru...
Abstract: Ectodermal dysplasia is a large heterogenous group of inherited disorders, defined by prim...
Background and Objective: The study was conducted to determine the occurrence and types of ophthalmo...
Abstract The Ectodermal Dysplasia comprises a large, heterogeneous group of inherited disorders that...
Purpose: To report a case of advanced childhood glaucoma secondary to congenital ectropion uveae (CE...
We report four cases of ectodermal dysplasia. Three of them are hypohidrotic ectodermal dysplasia (H...
The hypohidrotic ectodermal dysplasia (HED) is a rare genetic disease characterized by the absence o...
Hypohidrotic ectodermal dysplasia (HED), also known as Christ-Siemens-Touraine syndrome, is a rare X...
Ectodermal dysplasia is a hereditary disorder that occurs as a consequence of disturbances in the ec...
ABSTRACT Background and Setting: Hypohidrotic (anhidrotic) ectodermal dysplasia (HED) is a congenita...
Ectodermal dysplasia (ED) is a rare heterogenous group of ectodermal disorder, which primarily affec...
Ectodermal dysplasia is a hereditary disease characterized by a congenital dysplasia of one or more ...
Ichthyosiform dermatoses are a group of hereditary disorders characterized by dryness and roughness ...
Ectodermal dysplasia (ED) is a inherited genetic disorder with manifestations of abnormalities in mo...
Ectodermal dysplasia is a hereditary disorder that occurs as a consequence of disturbances in the ec...
Ectodermal dysplasia (ED) is a rare hereditary disorder involving two or more of the ectodermal stru...
Abstract: Ectodermal dysplasia is a large heterogenous group of inherited disorders, defined by prim...
Background and Objective: The study was conducted to determine the occurrence and types of ophthalmo...
Abstract The Ectodermal Dysplasia comprises a large, heterogeneous group of inherited disorders that...
Purpose: To report a case of advanced childhood glaucoma secondary to congenital ectropion uveae (CE...
We report four cases of ectodermal dysplasia. Three of them are hypohidrotic ectodermal dysplasia (H...
The hypohidrotic ectodermal dysplasia (HED) is a rare genetic disease characterized by the absence o...