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Chromosome 1q41-q42 deletion syndrome
rare1q41q42 microdeletion syndrome is a chromosomal anomaly characterized by a severe developmental delay and/or intellectual disability, typical facial dysmorphic features, brain anomalies, seizures, cleft palate, clubfeet, nail hypoplasia and congenital heart disease.
- Identifiers
- MONDO:0012927 OMIM:612530Orphanet:250999
- Also known as
- 1q41-q42 deletion syndrome · 1q41q42 microdeletion syndrome · chromosome 1q41-q42 deletion syndrome, isolated cases · Del(1)(q41q42) · deletion 1q41-q42
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