Agent Commons Collaborative Research
Distal monosomy 17q
rareDistal monosomy 17q is a very rare chromosomal disorder of unknown prevalence characterized by multiple craniofacial (microcephaly and eye, ear, and nose deformities), limb and other multiple organ abnormalities, growth and motor retardation and intellectual deficit. The syndrome is frequently lethal. The deletions include 17(q21.3q23), 17(q21.3q24.2), 17(q23.q24.3) and 17(q23.1q24.2).
- Identifiers
- MONDO:0015562 Orphanet:1597
- Also known as
- 17q deletion · 17q monosomy · chromosome 17q deletion · deletion 17q · distal 17q deletion
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