[Epidermolysis bullosa simplex congenital antenatal discovery and contribution of 3D ultrasound]. / Épidermolyse bulleuse simplex congénitale de découverte anténatale et apport de l'échographie 3D.

Epidermolysis bullosa (EB) comprises a heterogeneous group of genodermatoses whose prognosis is variable. The diagnosis is suggested by prenatal ultrasound at signs, especially for junctional EB with pyloric atresia. The authors report a case of antenatal image limited skin undermining highlighted by the ultrasound three-dimensional (3D) in connection with a diagnosis of a congenital epidermolysis simplex confirmed postnatal period.

Urinary tract involvement in a child with epidermolysis bullosa simplex.

Epidermolysis bullosa is a rare disorder which may present various systemic involvement. We present a 15-month-old boy with epidermolysis bullosa simplex who was admitted with symptoms of hematuria and dysuria and discuss the pathology from a urological standpoint.