NeurometPlus

Chromosome 12p deletion syndrome. 12p minus syndrome. Monosomy 12p.

Incidence

Very rare syndrome. Sporadic.

Clinical Characteristics

Deletion of the short arm of chromosome 12. The syndrome is relatively rare and has a variable phenotype, consisting of growth and mental retardation and various craniofacial, neurological, and other abnormalities.

Precipitants

None

Provocation Tests

None

Diagnostic Procedures

Karyotype. Deletion of the short arm of chromosome 12.

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