Other Names for this Disease
- De morsier syndrome
- Hypopituitarism and septooptic 'dysplasia'
- Septo-optic dysplasia with growth hormone deficiency
- Septooptic dysplasia
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Septo-optic dysplasia is usually sporadic, which means that the condition typically occurs in people with no history of the disorder in their family.
Less commonly, septo-optic dysplasia has been found to run in families. Most familial cases appear to have an autosomal recessive pattern of inheritance, which means that both copies of an associated gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the condition. In a few affected families, the disorder has had an autosomal dominant pattern of inheritance, which means one copy of an altered gene in each cell is sufficient to cause the condition.
- Septo-optic dysplasia. Genetics Home Reference. March 2010; http://ghr.nlm.nih.gov/condition/septo-optic-dysplasia. Accessed 7/13/2012.