Literature DB >> 13990468

The ocular manifestations of hereditary dystopic lipidosis (angiokeratoma corporis diffusum universale).

A N RAHMAN.   

Abstract

Entities:  

Keywords:  ANGIOKERATOMA; CORNEAL OPACITY; EYE MANIFESTATIONS; LIPOIDOSIS

Mesh：

Year:  1963        PMID： 13990468     DOI： 10.1001/archopht.1963.00960040714005

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


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  6 in total

1.  [On the etiology of dystrophia corneae verticillata].

Authors:  A Denden
Journal:  Albrecht Von Graefes Arch Klin Exp Ophthalmol       Date:  1966-04-18

2.  Angiokeratoma corporis diffusum. Some clinical aspects.

Authors:  A W Johnston; S D Weller; B J Warland
Journal:  Arch Dis Child       Date:  1968-02       Impact factor: 3.791

Review 3.  Ocular correlates of inborn metabolic defects.

Authors:  D G Cogan
Journal:  Can Med Assoc J       Date:  1966-11-19       Impact factor: 8.262

4.  X-chromosomal-linked diseases affecting the eye: status of the heterozygote female.

Authors:  A E Krill
Journal:  Trans Am Ophthalmol Soc       Date:  1969

5.  The Genetics of Angiokeratoma Corporis Diffusum (Fabry's Disease) and Its Linkage Relations with the Xg Locus.

Authors:  J M Opitz; F C Stiles; D Wise; R R Race; R Sanger; G R Von Gemmingen; R R Kierland; E G Cross; W P De Groot
Journal:  Am J Hum Genet       Date:  1965-07       Impact factor: 11.025

6.  [Cytogenetic study of a kinship with Fabry-Anderson syndrome (angiokeratoma corporis diffusion universale)].

Authors:  P Eberle; A Denden
Journal:  Albrecht Von Graefes Arch Klin Exp Ophthalmol       Date:  1969
  6 in total

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