Atlas of Ophthalmology

Anterior Chamber

Brain and Optical Pathway

Choroid

Anatomy and Embryology

Choroidal Dystrophy

Choroidal Folds (see also under Orbit, Sclera)

Ciliochoroidal Effusion

Congenital Anomalies (Abnormalities), Congenital Syndromes

Heredatitary Degenerations and Atrophy

Central Areolar Choroidal Atrophy (Sclerosis), Hereditary

Choroideremia (Colour Photography, FFA, OCT, ERG)

Choroideremia, Hereditary

Gyrate Atrophy with Hyperornithemia, Hereditary

Myopia

Infections, Systemic Disease

Surgical Procedures and Postoperative Cases

Trauma (Injury)

Tumor, Neoplasma

Vascular Diseases

Congenital Syndromes, Malformations and Abnomalities

Conjunctiva

Cornea

Glaucomas, Ocular Hypertension

Hypertensive Retinopathy

Iris and Ciliary Body

Strabismus, Ocular Motility Disorders

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Gyrate Atrophy with Hyperornithemia, Hereditary

Diagnosis:	Gyrate Atrophy with Hyperornithemia, Hereditary
Comment to photo:	Patchy chorioretinal atrophy. Concentrically restricted visual fields. Nightblindnes, Cataract. Fine hair, Muscle fatigue. Autosomal recessive.
Author(s):	Ruprecht, Klaus, Prof. Dr. med., Universitäts-Augenklinik, Homburg/Saar, Germany
ICD10-Code:	H31.22
Path:	Choroid -> Heredatitary Degenerations and Atrophy
Additional keywords:	choroid,
Image ID:	1881

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