Literature DB >> 985163

X-linked ocular albinism. An oculocutaneous macromelanosomal disorder.

F E O'Donnell, G W Hambrick, W R Green, W J Iliff, D L Stone.   

Abstract

Three unrelated kindreds with the Nettleship-Falls type of X-linked ocular albinism were studied. Postmortem examination of the eyes of an affected man revealed the presence of macromelanosomes in the pigment epithelia. Skin biopsy specimens of this patient, seven other affected male, and nine carrier female kindred members revealed the presence of Fontana-positive and dopa oxidase-positive macromelanosomes within the epidermis and dermis. Although clinically this disorder has been considered to be a form of albinism confined to the eyes, these findings indicate that an unusual disturbance in melanosome production characterized by macromelanosome formation affects the skin and the eyes. Histopathologic study of the skin is a useful adjunct in the diagnosis of X-linked ocular albinism, both in the affected and the carrier states. Linkage studies confirmed the close association of the Xg blood group with this disorder.

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Year:  1976        PMID: 985163     DOI: 10.1001/archopht.1976.03910040593001

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN: 0003-9950


  39 in total

1.  Genetic mapping of X linked ocular albinism: linkage analysis in British families.

Authors:  S J Charles; A T Moore; J R Yates
Journal:  J Med Genet       Date:  1992-08       Impact factor: 6.318

2.  An unconventional dileucine-based motif and a novel cytosolic motif are required for the lysosomal and melanosomal targeting of OA1.

Authors:  Rosanna Piccirillo; Ilaria Palmisano; Giulio Innamorati; Paola Bagnato; Domenico Altimare; Maria Vittoria Schiaffino
Journal:  J Cell Sci       Date:  2006-04-18       Impact factor: 5.285

3.  Abnormal crossing of the optic fibres shown by evoked magnetic fields in patients with ocular albinism with a novel mutation in the OA1 gene.

Authors:  L Lauronen; R Jalkanen; J Huttunen; E Carlsson; S Tuupanen; S Lindh; H Forsius; E-M Sankila; T Alitalo
Journal:  Br J Ophthalmol       Date:  2005-07       Impact factor: 4.638

4.  The protein Ocular albinism 1 is the orphan GPCR GPR143 and mediates depressor and bradycardic responses to DOPA in the nucleus tractus solitarii.

Authors:  Y Hiroshima; H Miyamoto; F Nakamura; D Masukawa; T Yamamoto; H Muraoka; M Kamiya; N Yamashita; T Suzuki; S Matsuzaki; I Endo; Y Goshima
Journal:  Br J Pharmacol       Date:  2014-01       Impact factor: 8.739

5.  An Xp22 microdeletion associated with ocular albinism and ichthyosis: approximation of breakpoints and estimation of deletion size by using cloned DNA probes and flow cytometry.

Authors:  R E Schnur; B J Trask; G van den Engh; H H Punnett; M Kistenmacher; M A Tomeo; R E Naids; R L Nussbaum
Journal:  Am J Hum Genet       Date:  1989-11       Impact factor: 11.025

Review 6.  Signaling pathways in melanosome biogenesis and pathology.

Authors:  Maria Vittoria Schiaffino
Journal:  Int J Biochem Cell Biol       Date:  2010-04-08       Impact factor: 5.085

7.  Pigmentation, pleiotropy, and genetic pathways in humans and mice.

Authors:  G S Barsh
Journal:  Am J Hum Genet       Date:  1995-10       Impact factor: 11.025

8.  Blue light hazard and aniridia.

Authors:  R V Abadi; C M Dickinson
Journal:  Br J Ophthalmol       Date:  1985-03       Impact factor: 4.638

9.  X linked ocular albinism in Japanese patients.

Authors:  T Shiono; M Tsunoda; Y Chida; M Nakazawa; M Tamai
Journal:  Br J Ophthalmol       Date:  1995-02       Impact factor: 4.638

10.  Visual insignificance of the foveal pit: reassessment of foveal hypoplasia as fovea plana.

Authors:  Michael F Marmor; Stacey S Choi; Robert J Zawadzki; John S Werner
Journal:  Arch Ophthalmol       Date:  2008-07
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