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

Endocrine Disorders

Hematopoesis

Immunologic Diseases

Amyloidosis, Familial

Case

Familial Amyloidosis

Familial Amyloidosis Skin Lesions

Familial Amyloidosis, Vitreous Opacity

Behcet Disease

Case: Dermatomyositis

Delayed recognition of forehead necrosis in Giant Cell Arteritis leading to permanent visual loss

Myasthenic Diplopia (Effect of Cold Test, Colour Image)

Okklusive Vaskulitis bei systemischem Lupus erythematodes (Farbbbild, FLA, OCT)

Rheumatic Diseases

Sarcoidosis

Scleroderma

Wegener's Granulomatosis

Infections

Mesenchyme and Skeleton

Metabolic Diseases

Normalbefunde, Visusminderung bei R/L Astigmatismus

Phakomatoses

Pseudoexfoliation Syndrome (PEX)

Endorsed by

iPod Podcasting

Familial Amyloidosis

Diagnosis:	Familial Amyloidosis
Comment to photo:	Attached to the posterior lens surface are fine white strands
Author(s):	Machemer, Robert, M.D., Duke Univ. Medical School, Durham, NC, USA
ICD10-Code:	E85.9
Path:	Systemic Diseases -> Immunologic Diseases -> Amyloidosis, Familial -> Case
Additional keywords:	vitreous, metabolic, systemic disease, pathognomonic
Image ID:	1505

-------------------------- -------------------------- -------------------------- -------------------------- -------------------------- -------------------------- -------------------------- -------------------------- -------------------------- -------------------------- -------------------------- --------------------------

Keyword-Associated

Information

>More Information

>Place an Advertisement

Your advertisement here >

Santen

Ophthalmology is our singular focus

read on