What causes Oculodentodigital dysplasia?
What causes Oculodentodigital dysplasia?
Oculodentodigital dysplasia is caused by changes ( mutations ) in the GJA1 gene . This gene provides instructions to the body to make a protein that helps to form gap junctions. Gap junctions allow for communication between cells of the body.
What is ODDD syndrome?
Oculodentodigital Syndrome (ODDD) is a Rare Genetic Condition Characterized by. A typical facial appearance. Variable eye, tooth and finger involvement.
What is Oculodentodigital syndrome (ODD)?
Oculodentodigital syndrome (ODD syndrome) is an extremely rare genetic condition that typically results in small eyes, underdeveloped teeth, and syndactyly and malformation of the fourth and fifth fingers. It has also been called oculo-dento-digital syndrome, oculodentodigital dysplasia (ODDD), and oculodentoosseous dysplasia (ODOD).
What is oculo-dento-digital dysplasia?
Oculo-dento-digital dysplasia is a rare disorder that may be inherited as an autosomal dominant trait or be caused by a new change in the genes that occurs for no apparent reason (mutation). There also have been a few instances in which it is thought to have been inherited as an autosomal recessive trait.
What are the treatment options for oculodentodigital dysplasia?
After a person is diagnosed with oculodentodigital dysplasia, there are a number of steps that can be taken in order to monitor other symptoms that may develop or to improve symptoms that are already occurring. For example, surgery may be recommended to correct syndactyly of the fingers or to remove bony growths.
What is ododdd syndrome?
ODDD Syndrome is a Rare Genetic Condition Characterized by. A typical facial appearance. Variable eye, tooth and finger involvement. Enamel hypoplasia. Selective missing teeth. Small teeth. Premature loss of teeth. Dental caries.
