Homozygous Epidermal Growth Factor Receptor (EGFR) mutation is associated with neonatal inflammatory skin and bowel disease type 2. We present the case of a preterm female infant with severe growth restriction and a severe and complex clinical course. She presented from birth with erosive and inflammatory skin lesions as well as several malformations (sparse scalp hair. craniofacial a... https://foldlyers.shop/product-category/house/