Oculocerebral cutaneous syndrome

Syn .: Delleman-Oorthuys syndrome.

Etiol .: Probably a lethal mutation with autosomal dominant inheritance, patients with mosaic-like type of inheritance survive.

Clinical: Skinless foci (defined as congenital skin atrophy, focal hypoplasia), brain malformations, cysts and numerous papillary protrusions around the orbits.

Lit .: [1] Inflammatory diseases of the cartilage. [In:] Braun-Falco O., Plewig G., Wolff HH, Burgdorf WHC: Dermatology, eds. half. Gliński W., Wolska H., Wydawnictwo Czelej, Lublin 2002, 807-10.

Source: A. Kaszuba, Z. Adamski: “Lexicon of dermatology”; XNUMXst edition, Czelej Publishing House

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