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Medical hypothesis, discovery & innovation ophthalmology journal, ISSN 2322-4436, 2014, Volume 3, Issue 3, p. 99
Journal Article
Journal of the Korean Ophthalmological Society, ISSN 0378-6471, 04/2013, Volume 54, Issue 4, pp. 667 - 670
To report the first case of lattice corneal dystrophy, gelsolin type in Korea. A 61-year-old man visited our clinic with severe dry eye symptom in both eyes.... 
Amyloidosis | Gelsolin | Lattice corneal dystrophy | Meretoja syndrome
Journal Article
대한안과학회지, ISSN 0378-6471, 2013, Volume 54, Issue 4, p. 667
Purpose: To report the first case of lattice corneal dystrophy, gelsolin type in Korea. Case summary: A 61-year-old man visited our clinic with severe dry eye... 
Amyloidosis | Gelsolin | Lattice corneal dystrophy | Meretoja syndrome
Journal Article
Muscle & Nerve, ISSN 0148-639X, 05/2016, Volume 53, Issue 5, pp. 762 - 769
IntroductionHereditary gelsolin amyloidosis (GA) is a rare condition caused by the gelsolin gene mutation. The diagnostic triad includes corneal lattice... 
cranial neuropathy | amyloidosis | gelsolin | bilateral facial paresis | facial paresis grading | Facial paresis grading | Amyloidosis | Gelsolin | Cranial neuropathy | Bilateral facial paresis | GSN GENE | NEUROSCIENCES | FINNISH TYPE FAF | POLYNEUROPATHY TYPE-IV | CLINICAL NEUROLOGY | LATTICE CORNEAL-DYSTROPHY | HEARING-LOSS | NEUROPATHY | FAMILIAL AMYLOIDOSIS | MERETOJAS SYNDROME | HEREDITARY AMYLOIDOSIS | MUTATION | Wood products | Workshops | Cornea | Motor units | Muscles | Facial nerve | Acoustics | Surgery | Cranial nerves | Point mutation | Skin | Dystrophy | Age | Injuries | EMG | Bell's palsy | Vestibulocochlear Nerve Diseases - physiopathology | Cutis Laxa - etiology | Humans | Middle Aged | Vestibulocochlear Nerve Diseases - etiology | Oculomotor Nerve Diseases - etiology | Male | Amyloid Neuropathies, Familial - physiopathology | Facial Nerve Diseases - etiology | Hypoglossal Nerve Diseases - physiopathology | Corneal Dystrophies, Hereditary - physiopathology | Facial Paralysis - physiopathology | Aged, 80 and over | Adult | Female | Electromyography | Amyloidosis - complications | Cranial Nerve Diseases - physiopathology | Hypoglossal Nerve Diseases - etiology | Trigeminal Nerve Diseases - physiopathology | Trigeminal Nerve Diseases - etiology | Amyloid Neuropathies, Familial - complications | Amyloidosis - physiopathology | Neural Conduction | Facial Nerve Diseases - physiopathology | Oculomotor Nerve Diseases - physiopathology | Facial Muscles - physiopathology | Cranial Nerve Diseases - etiology | Corneal Dystrophies, Hereditary - complications | Aged | Facial Paralysis - etiology | Development and progression | Paralysis, Facial | Gene mutations | Index Medicus
Journal Article
Case Reports in Ophthalmology, ISSN 1663-2699, 05/2017, Volume 8, Issue 2, pp. 446 - 451
Familial amyloidosis of the Finnish type or Meretoja syndrome is a rare autosomic dominant inherited systemic condition. It was first described by Meretoja in... 
Familial amyloidosis | Corneal pathology | Gelsolin | Lattice corneal dystrophy | Meretoja syndrome | Finnish type | Pathology | Genetic counseling | Genetic testing | Mutation | Deoxyribonucleic acid--DNA | Familial amyloidosis, Finnish type
Journal Article
Ophthalmology, ISSN 0161-6420, 12/1983, Volume 90, Issue 12, pp. 1512 - 1517
Journal Article
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