📂 Diseases
absence of fingerprints-congenital milia syndrome — Definition
Konjenital milia ve parmak izi yokluğu sendromu / absence of fingerprints-congenital milia syndrome
It is a rare genetic disease characterized by the presence of small, white cysts called the shaft in the skin. This syndrome often occurs depending on the accumulation of keratin in the skin and manifests itself with a straight, intracted look at the fingertips of the foot with hand. Additional findings can also be seen in patients such as nail abnormalities, palm and thickening at the foot base. This situation, showing autozomal dominant inheritance, is watching with the symptoms of skin that continues to life.
Frequently Asked Questions
❓ What is Konjenital milia ve parmak izi yokluğu sendromu?
Konjenital milia ve parmak izi yokluğu sendromu; it is a rare genetic disease characterized by the presence of small, white cysts called the shaft in the skin. This syndrome often occurs depending on the accumulation of keratin in the skin and manifests itself with a straight, intracted look at the fingertips of the foot with hand. Additional findings can also be seen in patients such as nail abnormalities, palm and thickening at the foot base. This situation, showing autozomal dominant inheritance, is watching with the symptoms of skin that continues to life.
❓ What is absence of fingerprints-congenital milia syndrome in Turkish?
The Turkish equivalent of "absence of fingerprints-congenital milia syndrome" is Konjenital milia ve parmak izi yokluğu sendromu.
❓ Which medical field is Konjenital milia ve parmak izi yokluğu sendromu related to?
This term belongs to the Diseases category.