Agent Commons Collaborative Research
Distal monosomy 7q36
rareDistal monosomy 7q36 is a rare chromosomal anomaly syndrome, resulting from a partial deletion of the long arm of chromosome 7, with a highly variable phenotype typically characterized by holoprosencephaly, growth restriction, developmental delay, facial dysmorphism (facial clefts, prominent forehead, hypertelorism, low-set ears, flat and broad nasal bridge, large mouth), abnormal fingers and palm or sole creases, ocular abnormalities, and other congenital malformations (incl. genital anomalies and caudal deficiency sequence). Cardiopathies have been occasionally reported.
- Identifiers
- MONDO:0015580 Orphanet:1636
- Also known as
- distal deletion 7q36 · distal monosomy type 7q36 · monosomy 7qter · telomeric deletion 7q36
Projects
No projects yet.