Template:Trisomy 18 features table

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Frequency Organ/System Prevalent type of malformation
Common (>75%) heart septal defects, patent ductus arteriosus, and polyvalvular disease
Frequent (25-75%) genitourinary horseshoe kidney
Less frequent (5-25%) gastrointestinal

central nervous system

craniofacial

eye

limb

omphalocele, esophageal atresia with tracheo-esophageal fistula, pyloric stenosis, Meckel diverticulum

cerebellar hypoplasia, agenesis of corpus callosum, polymicrogyria, spina bifida

orofacial clefts

microphthalmia, coloboma, cataract, corneal opacities

radial aplasia/hypoplasia

Table modified from[1]
  1. ↑ Cereda A & Carey JC. (2012). The trisomy 18 syndrome. Orphanet J Rare Dis , 7, 81. PMID: 23088440 DOI.