Barber–Say syndrome
Medical condition
From Wikipedia, the free encyclopedia
Barber-Say syndrome (BSS) is a very rare congenital disorder associated with excessive hair growth (hypertrichosis), fragile (atrophic) skin, eyelid deformities (ectropion), and an overly broad mouth (macrostomia).[1]
| Barber Say syndrome | |
|---|---|
| Other names | Hypertrichosis-atrophic skin-ectropion-macrostomia syndrome |
| |
| Barber-Say syndrome has an autosomal dominant pattern of inheritance | |
| Usual onset | Neonatal |
| Differential diagnosis | Treacher Collins syndrome |
Barber-Say syndrome is phenotypically similar to Ablepharon macrostomia syndrome, which is also associated with dominant mutations in TWIST2.[2]
Signs and symptoms
- Severe hypertrichosis, especially of the back
- Skin abnormalities, including hyperlaxity and redundancy
- Facial dysmorphism, including macrostomia
- Eyelid deformities
- Abnormal and low-set ears
- Bulbous nasal tip with hypoplastic alae nasi
- Low frontal hairline
Genetics
Multiple cases of parent-to-child transmission suggest that Barber-Say syndrome exhibits autosomal dominant inheritance.[3] Exome sequencing and expression studies have shown that BSS is caused by mutations in the TWIST2 gene that affect a highly conserved residue of TWIST2 (twist-related protein 2). TWIST2 is a basic helix-loop-helix transcription factor that binds to E-box DNA motifs (5'-CANNTG-3') as a heterodimer and inhibits transcriptional activation.[4] Because TWIST2 mediates mesenchymal stem cell differentiation[5] and prevents premature or ectopic osteoblast differentiation,[6] mutations in TWIST2 that disrupt these functions by altering DNA-binding activity could explain many of the phenotypes of BSS.[2]