Educational Content: This article is for informational purposes only and does not constitute medical advice. Always consult a healthcare provider for diagnosis and treatment.
Definition of Strømme syndrome (Stromme)
Medically reviewed by Min Clinic Staff | Updated: January 2026
Strømme syndrome: a rare genetic condition characterized by birth defects or abnormalities in the eyes, intestines, and skull. The abnormalities vary among affected people, and sometimes problems with the kidneys or heart are also present. The condition results from a mutation in a gene known as CENPF, and it is inherited in an autosomal recessive manner, meaning that to be affected, an individual must receive a copy of the defective gene from each parent.
