Gordon K, Siu V M, Sergovich F, Jung J
Department of Pediatrics, Dalhousie University, Halifax, Nova Scotia, Canada.
Am J Med Genet. 1993 Apr 15;46(2):142-4. doi: 10.1002/ajmg.1320460208.
Rett syndrome consists of a characteristic progressive encephalopathy in females. The cause of this syndrome is unknown. We present a patient with 18q-mosaicism who, along with the characteristics of this autosomal deletion, also fulfills the clinical criteria for Rett syndrome. This may demonstrate heterogeneity within this as yet clinically defined syndrome. A thorough chromosomal analysis should be performed in suspected cases of Rett syndrome.