Meretoja Syndrome (Finnish Type, FAP IV) 7
General: Lattice corneal dystrophy type II with familial amyloid polyneuropa 454j92e thy type IV; also called primary hereditary systemic amyloidosis.
Ocular: Lattice corneal dystrophy; cranial nerve palsies.
Clinical: Multiple neurologic symptoms such as severe itching, various nerve palsies, and diminished vibratory sensation; patients are said to develop a so-called bloodhound-like appearance due to skin and facial nerve degeneration.
Asaoka T, et al. Lattice corneal dystrophy type II with familial amyloid polyneuropa 454j92e thy type IV. Jpn J Ophthalmol 1993; 37:426-431.
Purcell JJ, et al. Lattice corneal dystrophy associated with familial systemic amyloidosis (Meretoja's syndrome). Ophthalmology 1983; 90:1512-l517.
Rintala AE, et al. Primary hereditary systemic amyloidosis (Meretoja's syndrome): clinical features and treatment by plastic surgery. Scand J Plast Reconstr Surg Hand Surg 1988; 22:141-l45.
Hermit Syndrome [...] |
Optic Atrophy with Demyelinating Disease of CNS General: Autosom [...] |
Pelizaeus-Merzbacher Disease (Aplasia Axialis Extracorticalis Congenita; Sudanophilic Leukodystrophy) [...] |
Copyright © 2010 - 2024
: eSanatos.com - Reproducerea, chiar si partiala, a materialelor de pe acest site este interzisa!
Informatiile medicale au scop informativ si educational. Ele nu pot inlocui consultul medicului si nici diagnosticul stabilit in urma investigatiilor si analizelor medicale la un medic specialist.
Termeni si conditii - Confidentialitatea datelor - Contact
Despre diseases |
| Alte sectiuni |
|
Ai o problema medicala? |
