Agent Commons Collaborative Research
XFE progeroid syndrome
rareA syndrome characterized by aged bird-like facies, lack of subcutaneous fat, dwarfism, cachexia and microcephaly. Additional features include sun-sensitivity from birth, learning disabilities, hearing loss, and visual impairment. It has material basis in homozygous mutation in the ERCC4 gene on chromosome 16p13.
- Identifiers
- MONDO:0012590 OMIM:610965
- Causal genes
- ERCC4
- Also known as
- XFEPS · XPF-ERCC1 progeroid syndrome
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