Синдром лінійного кератозу-вродженого іхтіозу- склерозуючої кератодермії
ORPHA:281201· ICD-10 Q82.8· Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome
Визначення(English summary)
Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome is an inherited epidermal disorder characterized by palmoplantar keratoderma, linear hyperkeratotic papules on the flexural side of large joints (cord-like distribution around wrists, in antecubital and popliteal folds), hyperkeratotic plaques (on neck, axillae, elbows, wrists, and knees), mild ichthyosiform scaling, and sclerotic constrictions around fingers that present flexural deformities.
- Поширеність
- Unknown
- Успадкування
- Autosomal recessive
- Вік початку
- Infancy, Neonatal