ABSTRACT
Neurological abnormalities have been occasionally associated with Leber's hereditary optic neuropathy (LHON). We describe four patients with spastic dystonia from two of our 35 LHON families. Magnetic resonance imaging revealed signal alterations of globus pallidus, putamen, internal capsula, and substantia nigra. Neuropathological findings in one of the patients with dystonia are described. Each of the dystonia families carries a different mtDNA mutation; one at np 3460 and one at np 11778. Periventricular multiple sclerosis-like white matter lesions were observed in one individual from a third family with the mtDNA 3460 mutation. Neurological disorders are probably underestimated in association with LHON.
Subject(s)
Brain Diseases/genetics , DNA, Mitochondrial , Optic Atrophies, Hereditary/genetics , Adolescent , Adult , Brain/pathology , Brain Diseases/diagnosis , Child , DNA Mutational Analysis , Dystonia/genetics , Female , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Optic Atrophies, Hereditary/complications , Optic Atrophies, Hereditary/diagnosis , Pedigree , Point Mutation/geneticsABSTRACT
A thirty-eight year-old man, treated medically since 1985 for a chronic pancreatitis, showed a choroidal infiltrate in the superior mid periphery of the left fundus. A thorough systemic examination could not reveal an underlying cause. The differential diagnosis of the lesion included metastasis, intraocular lymphoma and sarcoidosis. Two months later the lesion had increased both on fundoscopy and echography and was accompanied by a serous macular detachment. A choroidal biopsy showed a moderately well differentiated mucinous adenocarcinoma. The primary site could not be determined. The mucinous character is rather suggestive for a gastrointestinal origin. Gastro intestinal choroidal metastases, and more specifically the pancreatic ones, are however rare.
Subject(s)
Adenocarcinoma/pathology , Adenocarcinoma/secondary , Choroid Neoplasms/pathology , Choroid Neoplasms/secondary , Neoplasms, Unknown Primary , Adult , Biopsy , Humans , MaleABSTRACT
The clinical and genetical manifestations of 64 patients of 34 families with LHON, taken up in an ophthalmogenetic register for LHON, are discussed. The disorder appeared to occur sporadically in 41.2% of the patients. Genotypic characteristics of the pedigrees revealed the 11778 mutation in 57.5% of the families, the 3460 mutation in 21.2% and the 15257 mutation in 9.1%. One family carried only a secondary mutation pattern. Fourteen percent of patients with the 11778 mutation showed recovery of their visual acuity. Visual recovery with the 3460 and 15257 mutation was respectively 21% and 33%. Our youngest patient was 4 years old.
Subject(s)
Optic Atrophies, Hereditary/genetics , Point Mutation , Adolescent , Adult , Child , Child, Preschool , Female , Fluorescein Angiography , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Optic Atrophies, Hereditary/diagnosis , Optic Atrophies, Hereditary/physiopathology , Ultrasonography , Visual AcuityABSTRACT
Congenital ectropion uveae (CEU) is a rare, non progressive anomaly characterised by the presence of iris pigment epithelium on the anterior surface, an anterior iris insertion, dysgenesis of the drainage angle and glaucoma. The condition is characteristically unilateral and rarely hereditary. The current theory of development arrest is discussed. We report three cases with CEU of which two already developed glaucoma. All patients with CEU should be carefully examined periodically to detect glaucoma.
Subject(s)
Ectropion/congenital , Uveal Diseases/congenital , Child , Ectropion/complications , Ectropion/diagnosis , Female , Glaucoma/etiology , Glaucoma/surgery , Humans , Infant , Male , Middle Aged , Trabeculectomy , Uveal Diseases/diagnosisABSTRACT
The detection of hidden visual loss is important in establishing the diagnosis of multiple sclerosis, especially in patients who have neurologic symptoms of the disease. Both visual evoked potentials and contrast sensitivity have been used for this purpose. We compared the sensitivities of pattern-reversal visual evoked potentials and contrast sensitivity, measured with the Vistech VCTS 6500 chart, in detecting hidden visual loss in 18 patients with multiple sclerosis whose visual acuity was correctable to 20/20 (6/6) or better in the examined eye. Thirteen patients had delayed visual evoked potential latencies. An additional four patients had reduced P100 amplitudes without prolonged latencies. Nine patients had abnormal contrast sensitivity. The visual evoked potential was more sensitive than contrast sensitivity at detecting hidden visual loss in patients with multiple sclerosis (p less than 0.01).
Subject(s)
Contrast Sensitivity , Evoked Potentials, Visual , Multiple Sclerosis/physiopathology , Vision Disorders/physiopathology , Adult , Female , Humans , Male , Middle Aged , Pattern Recognition, Visual , Sensitivity and Specificity , Visual AcuityABSTRACT
The sensitivity of the VISTECH chart in the detection of hidden visual loss is debated. We tried to evaluate the diagnostic value of the test by using different illumination levels. Twelve MS-patients with normal acuity but a pathological VEP were examined at 9 different illuminations. We did not identify more abnormalities among patients, using VISTECH test at other illumination levels than the one recommended by the manufacturer.
