NISBD1 is an extremely rare disorder of neonatal onset characterized by life-long inflammation affecting the skin, hair and gut. Children are affected with diarrhea that worsens in parallel with increases in severity of skin disease.
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
Certain disorders involving the immune mechanism
Autosomal recessive
2p25.1
NISBD1 is an extremely rare disorder of neonatal onset characterized by life-long inflammation affecting the skin, hair and gut. Children are affected with diarrhea that worsens in parallel with increases in severity of skin disease.