Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency
ORPHA:91135· ICD-10 D68.4
Definition
A rare genetic skin disease characterized by severe skin laxity affecting the trunk and limbs.
- Prevalence
- <1 / 1 000 000
- Inheritance
- Autosomal recessive, Unknown
- Age of onset
- Adolescent, Childhood