NeurometPlus

Chromosome 6p deletion syndrome. 6p minus syndrome. Monosomy 6p.

Incidence

Very rare syndrome. Sporadic.

Clinical Characteristics

Deletion of the short arm of chromosome 6 with variable abnormalities, including mental retardation, microcephaly, abnormal cranial sutures, broad nasal bridge, ear and eye anomalies, short neck, pectus excavatum, Poland anomaly (absence of the pectoralis major muscle of its sternal portion associated with ipsilateral shortening of the phalanges with syndactyly), deafness, congenital heart defects, and highly arched palate.

Precipitants

None

Provocation Tests

None

Diagnostic Procedures

Karyotype. Deletion of the short arm of chromosome 6.

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