46,XX Gonadal Dysgenesis Epibulbar Dermoid

Overview

Type of disease: Rare conditions

46 XX gondal dysgenesis epibulbar dermoid is a rare genetic condition. This condition results from a mutation or error in a person’s DNA or genes. This can cause birth defects such as infertility and no secondary sex characteristics, as well as epibulbar dermoid (an eye disorder), deafness, and skin tags. Although there is currently no cure for 46 XX gondal dysgenesis epibulbar dermoid, there are various resources to help manage the condition and treat birth defects. For example, surgical removal is possible for skin tags and speech therapists are helpful for individuals affected by deafness. Doctors seek help from various therapists and community services to provide support and care for families affected by 46 XX gondal dysgenesis epibulbar dermoid.

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