CLOVES syndrome.
review · Level V
Where this comes from
- Record sourced from PubMed, PMID 24161472.
- Also identified by DOI 10.1016/j.jhsa.2013.08.120.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
A cohort of patients with overgrowth syndromes has been identified with congenital lipomatous overgrowth, dysregulated fat deposits, and mixed vascular malformations. The acronym CLOVES was given on a heuristic basis to stand for congenital lipomatous overgrowth (CLO), vascular malformation (V), epidermal nevi (E), and scoliosis and spinal deformities (S). These patients have upper limb anomalies with variable phenotypes. Although hand anomalies alone cannot make the diagnosis, the foot, truncal, cutaneous and spinal anomalies are particularly diagnostic. CLOVES syndrome has emerged as a distinct clinical entity diagnosed by clinical and radiographic examinations. The overgrowth pattern is now easily distinguished from other overgrowth syndromes.
Medical subject headings
- Abnormalities, Multiple
- Hand Deformities, Congenital
- Lipoma
- Musculoskeletal Abnormalities
- Nevus
- Vascular Malformations
Anatomy
- hand