📂 Diseases
Hypopigmentation-punctate palmoplantar keratoderma syndrome — Definition
Hipopigmentasyon-noktasal palmoplantar keratoderma sendromu / Hypopigmentation-punctate palmoplantar keratoderma syndrome
It is a rare genetic skin disease characterized by nucleusal thickening (keratoderma) in the palm and foot bases. Lesions often show symmetrical distribution and appear in the form of small, hard-papular. The disease autozomal dominant inheritance exhibits paterni and often becomes pronounced during childhood or puberty. Clinically, skin changes in the hands and feet can cause pain and walking strength.
Frequently Asked Questions
❓ What is Hipopigmentasyon-noktasal palmoplantar keratoderma sendromu?
Hipopigmentasyon-noktasal palmoplantar keratoderma sendromu; it is a rare genetic skin disease characterized by nucleusal thickening (keratoderma) in the palm and foot bases. Lesions often show symmetrical distribution and appear in the form of small, hard-papular. The disease autozomal dominant inheritance exhibits paterni and often becomes pronounced during childhood or puberty. Clinically, skin changes in the hands and feet can cause pain and walking strength.
❓ What is Hypopigmentation-punctate palmoplantar keratoderma syndrome in Turkish?
The Turkish equivalent of "Hypopigmentation-punctate palmoplantar keratoderma syndrome" is Hipopigmentasyon-noktasal palmoplantar keratoderma sendromu.
❓ Which medical field is Hipopigmentasyon-noktasal palmoplantar keratoderma sendromu related to?
This term belongs to the Diseases category.