📂 Diseases
congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome — Definition
Konjenital nefrotik sendrom-interstisyel akciğer hastalığı-epidermolizis bülloza sendromu / congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome
This syndrome is a rare genetic disease characterized by nephrotic syndrome (proteinurity, edema), interstitial fibrosis in the lungs (nefes millet, cough) and epidermolizis butlloza (colayca water collection and peeling) in the skin. Usually autozomal indicates resessive inheritance and leads to serious complications in early periods of life. Treatment is symptomatic and supporting; kidney failure and respiratory problems are often seen.
Frequently Asked Questions
❓ What is Konjenital nefrotik sendrom-interstisyel akciğer hastalığı-epidermolizis bülloza sendromu?
Konjenital nefrotik sendrom-interstisyel akciğer hastalığı-epidermolizis bülloza sendromu; this syndrome is a rare genetic disease characterized by nephrotic syndrome (proteinurity, edema), interstitial fibrosis in the lungs (nefes millet, cough) and epidermolizis butlloza (colayca water collection and peeling) in the skin. Usually autozomal indicates resessive inheritance and leads to serious complications in early periods of life. Treatment is symptomatic and supporting; kidney failure and respiratory problems are often seen.
❓ What is congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome in Turkish?
The Turkish equivalent of "congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome" is Konjenital nefrotik sendrom-interstisyel akciğer hastalığı-epidermolizis bülloza sendromu.
❓ Which medical field is Konjenital nefrotik sendrom-interstisyel akciğer hastalığı-epidermolizis bülloza sendromu related to?
This term belongs to the Diseases category.