Fokale dermaIe Hypoplasie mit Keratokonus, Ösophaguspapillomen und Hidrokystomen

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Abstract
Focal dermal hypoplasia (Goltz’s syndrome, Goltz-Gorlin syndrome), an uncommon malady belonging to the group of congenital poikiloderma, is characterized by its broad spectrum of meso-ectodermal defects involving the skin as well as the eyes, skeletal system and teeth. The case represented here is identical with the one published by Naegeli 1926, and contains some additional findings that have not yet been reported, namely: multiple hidrocystomas, bilateral keratoconus, papillomatosis of esophagus, hiatus hernia.

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