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GuideWisdom™

This WisdomCard managed by: Tara Salamone

18p minus syndrome, or chromosome 18p partial monosomy, is a genetic anomaly which occurs when a portion of the short arm is missing or deleted from one of the pair of chromosome 18. Persons with 18p minus syndrome may have different medical and developmental concerns; most are characterized with mental impairment, speech delay, and short stature. Other common problems include near- or far-sightedness, ear infection, and cleft lip and palate; heart defects are also common. Regular medical consultation is advised.

Top Resources on 18p Minus Syndrome

• Chromosome 18 Registry & Research Society: 18p- Introduction
• National Organization for Rare Disorders: Chromosome 18, Monosomy 18p
• Genetics Home Reference: What Chromosomal Conditions are Related to Chromosome 18?
• WrongDiagnosis: 18p Minus Syndrome
• DiagnosisPro: Disease Information for 18p Chromosome Deletion Complex]

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