Atlas of Ophthalmology

Anterior Chamber

Brain and Optical Pathway

Choroid

Congenital Syndromes, Malformations and Abnomalities

Conjunctiva

Cornea

Glaucomas, Ocular Hypertension

Hypertensive Retinopathy

Iris and Ciliary Body

Strabismus, Ocular Motility Disorders

Systemic Diseases

Diseases of the Digestive Tract

Mesenchyme and Skeleton

Metabolic Diseases

Normalbefunde, Visusminderung bei R/L Astigmatismus

Phakomatoses

Pseudoexfoliation Syndrome (PEX)

Skin

Cataracta syndermatotica in Skin Diseases

Cicatricial ectropion in congenital ichthyosis (Collodion Baby)

Hypertrophic Osteoarthropathy (HOA) (Pachydermoperiostitis)

Ichthyosis

Melkersson-Rosenthal-Syndrome

Pseudoxanthoma Elasticum, Grönblad-Strandberg Syndrome

Xanthogranuloma

Xeroderma pigmentosum

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Melkersson-Rosenthal-Syndrome

Diagnosis:	Melkersson-Rosenthal-Syndrome
Comment to photo:	Granulomatous inflammation and fibrosis of unknown origin of the skin of face and of the tissues of the mouth. Here the lids are mostly affected. (G.O.H. Naumann)
Author(s):	Nover, Arno, Prof. Dr., EOPS 1975, Mainz, Germany
ICD10-Code:	L92.8
Path:	Systemic Diseases -> Skin
Additional keywords:	Immun
Image ID:	5883

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