Literature DB >> 3713758

Abnormalities of the central visual pathways in Prader-Willi syndrome associated with hypopigmentation.

D J Creel, C M Bendel, G L Wiesner, J D Wirtschafter, D C Arthur, R A King.   

Abstract

Patients with oculocutaneous or ocular albinism have misrouting of optic fibers, with fibers from 20 degrees or more of the temporal retina crossing at the chiasm instead of projecting to the ipsilateral hemisphere. Misrouting can result in strabismus and nystagmus. Because patients with the Prader-Willi syndrome may also have hypopigmentation and strabismus, we wondered whether they too might have misrouting of optic fibers. We therefore studied six patients with Prader-Willi syndrome selected for a history of strabismus, using pattern-onset visually evoked potentials with binocular and monocular stimulation to look for evidence of misrouted retinal-ganglion fibers. Four had hypopigmentation, and three of these four had abnormal evoked potentials indistinguishable from those recorded in human albinos. The two with normal pigmentation had normal responses. These findings indicate that patients with Prader-Willi syndrome who have hypopigmentation have a brain abnormality characterized by misrouting of retinal-ganglion fibers at the optic chiasm--a finding previously reported only in forms of albinism.

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Year:  1986        PMID: 3713758     DOI: 10.1056/NEJM198606193142503

Source DB:  PubMed          Journal:  N Engl J Med        ISSN: 0028-4793            Impact factor:   91.245


  16 in total

Review 1.  Oculocutaneous albinism.

Authors:  S Biswas; I C Lloyd
Journal:  Arch Dis Child       Date:  1999-06       Impact factor: 3.791

2.  The p locus is closely linked to the mouse homolog of a gene from the Prader-Willi chromosomal region.

Authors:  Y Nakatsu; Y Gondo; M H Brilliant
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

3.  The tyrosinase-positive oculocutaneous albinism locus maps to chromosome 15q11.2-q12.

Authors:  M Ramsay; M A Colman; G Stevens; E Zwane; J Kromberg; M Farrall; T Jenkins
Journal:  Am J Hum Genet       Date:  1992-10       Impact factor: 11.025

4.  Synchrony of oculocutaneous albinism, the Prader-Willi syndrome, and a normal karyotype.

Authors:  C E Wallis; P H Beighton
Journal:  J Med Genet       Date:  1989-05       Impact factor: 6.318

5.  Visual evoked potentials in Negro carriers of the gene for tyrosinase positive oculocutaneous albinism.

Authors:  D Castle; J Kromberg; R Kowalsky; R Moosa; N Gillman; E Zwane; V Fritz
Journal:  J Med Genet       Date:  1988-12       Impact factor: 6.318

Review 6.  The mouse pink-eyed dilution locus: a model for aspects of Prader-Willi syndrome, Angelman syndrome, and a form of hypomelanosis of Ito.

Authors:  M H Brilliant
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

7.  Prader-Willi Syndrome: Clinical and Genetic Findings.

Authors:  Merlin G Butler; Travis Thompson
Journal:  Endocrinologist       Date:  2000-07

8.  Prader-Willi syndrome: current understanding of cause and diagnosis.

Authors:  M G Butler
Journal:  Am J Med Genet       Date:  1990-03

9.  Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome.

Authors:  M G Butler
Journal:  Am J Hum Genet       Date:  1989-07       Impact factor: 11.025

10.  Hypopigmentation in the Prader-Willi syndrome.

Authors:  G L Wiesner; C M Bendel; D P Olds; J G White; D C Arthur; D W Ball; R A King
Journal:  Am J Hum Genet       Date:  1987-05       Impact factor: 11.025

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