Literature DB >> 3766665

Ophthalmologic and systemic manifestations of Alström's disease.

R H Millay, R G Weleber, J R Heckenlively.   

Abstract

Alström's syndrome consists of pigmentary retinopathy, diabetes, obesity, normal mental capacity, and sensorineural deafness. The early retinal findings are optic atrophy, salt-and-pepper pigment epithelial abnormalities, and marked vascular attenuation. Later in the disease process, diffuse areas of chorioretinal atrophy and large clumps of pigment develop. Severe visual loss in the first decade is characteristic and is an important point in the differential diagnosis. Clinically evident renal disease is a variable age-related phenomenon, and is probably the most frequent cause of death.

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Year:  1986        PMID: 3766665     DOI: 10.1016/0002-9394(86)90078-4

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  9 in total

1.  A patient with features of both Bardet-Biedl and Alström syndromes.

Authors:  C Hauser; C Rojas; A Roth; E Schmied; J H Saurat
Journal:  Eur J Pediatr       Date:  1990-08       Impact factor: 3.183

2.  Alstrom's syndrome: further evidence of autosomal recessive inheritance and endocrinological dysfunction.

Authors:  S J Charles; A T Moore; J R Yates; T Green; P Clark
Journal:  J Med Genet       Date:  1990-09       Impact factor: 6.318

3.  Molecular advances in retinitis pigmentosa.

Authors:  R G Weleber; W H Murphey
Journal:  West J Med       Date:  1991-10

4.  [Alström syndrome--a rare disease of diabetic association].

Authors:  B Weichenhain; J Stemplinger; A G Ziegler; W Rabl; E Standl; H Stiegler
Journal:  Med Klin (Munich)       Date:  1997-03-15

Review 5.  Retinitis pigmentosa, pigmentary retinopathies, and neurologic diseases.

Authors:  M Tariq Bhatti
Journal:  Curr Neurol Neurosci Rep       Date:  2006-09       Impact factor: 5.081

6.  Spectral-domain optical coherence tomography findings in Alström syndrome.

Authors:  Gad Dotan; Vikas Khetan; Jan D Marshall; Elizabeth Affel; Denise Armiger-George; Jürgen K Naggert; Gayle B Collin; Alex V Levin
Journal:  Ophthalmic Genet       Date:  2017-01-23       Impact factor: 1.803

7.  Fundus changes in mesangiocapillary glomerulonephritis type II: clinical and fluorescein angiographic findings.

Authors:  J Duvall-Young; C D Short; M F Raines; R Gokal; W Lawler
Journal:  Br J Ophthalmol       Date:  1989-11       Impact factor: 4.638

8.  A case report of two siblings with Alstrom syndrome without hearing loss associated with two new ALMS1 variants.

Authors:  Maria F Shurygina; Maria A Parker; Catie L Schlechter; Rui Chen; Yumei Li; Richard G Weleber; Paul Yang; Mark E Pennesi
Journal:  BMC Ophthalmol       Date:  2019-12-07       Impact factor: 2.209

9.  Prevalence and associated relating factors in patients with hereditary retinal dystrophy: a nationwide population-based study in Taiwan.

Authors:  Peng Yeong Woon; Jia-Ying Chien; Jen-Hung Wang; Yu-Yau Chou; Mei-Chen Lin; Shun-Ping Huang
Journal:  BMJ Open       Date:  2022-04-08       Impact factor: 2.692

  9 in total

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