The purpose of this overview is to increase the awareness of clinicians regarding the clinical characteristics of primary mitochondrial disorders, their diagnosis, and management, and to inform genetic counseling of individuals with a primary mitochondrial disorder and their family members. The following are the goals of this overview.
Goal 1: Describe the clinical characteristics of primary mitochondrial disorders.
Goal 2: Provide evaluation strategies to identify the genetic cause of a primary mitochondrial disorder in a proband.
Goal 3: Identify patient care guidelines for primary mitochondrial disorders.
Goal 4: Inform genetic counseling of family members of an individual with a primary mitochondrial disorder.
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