Literature DB >> 1018304

Lowe's syndrome: identification of carriers by lens examination.

R J Gardner, N Brown.   

Abstract

Lens examinations were performed on 7 obligate and 7 possible carriers of the X-linked gene for Lowe's syndrome, and on 117 controls. By quantitatively grading punctate cortical opacities, it was possible to discriminate between the obligate carriers and the controls with a fair degree of confidence. In the age group most important for genetic counselling, that of child bearing, the data are too limited for the derivation of precise estimates, but may, nevertheless, be useful. More such data are needed.

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Year:  1976        PMID: 1018304      PMCID: PMC1013469          DOI: 10.1136/jmg.13.6.449

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  7 in total

1.  LOWE'S SYNDROME.

Authors:  J B DUNDAS
Journal:  Proc R Soc Med       Date:  1964-09

2.  Symposium on metabolic diseases of the eye, Cystinosis. Ocule-cerebro-renal (Lowe's) syndrome.

Authors:  D P GREAVES
Journal:  Proc R Soc Med       Date:  1963-01

3.  Two children with the oculo-cerebrorenal syndrome of Lowe, Terrey and MacLachlan.

Authors:  C E DENT; J M SMELLIE
Journal:  Proc R Soc Med       Date:  1961-04

4.  Lowe syndrome: identification of the carrier state.

Authors:  N Brown; R J Gardner
Journal:  Birth Defects Orig Artic Ser       Date:  1976

5.  An advanced slit-image camera.

Authors:  N Brown
Journal:  Br J Ophthalmol       Date:  1972-08       Impact factor: 4.638

6.  Macrophotography of the anterior segment of the eye.

Authors:  N Brown
Journal:  Br J Ophthalmol       Date:  1970-10       Impact factor: 4.638

7.  Lowe's syndrome: a search or the carrier state.

Authors:  L B Holmes; B L McGowan; M L Efron
Journal:  Pediatrics       Date:  1969-09       Impact factor: 7.124

  7 in total
  10 in total

Review 1.  Gene mapping of mineral metabolic disorders.

Authors:  R V Thakker; K E Davies; J L O'Riordan
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

Review 2.  X linked mental retardation.

Authors:  I A Glass
Journal:  J Med Genet       Date:  1991-06       Impact factor: 6.318

3.  Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.

Authors:  R A Lewis
Journal:  Trans Am Ophthalmol Soc       Date:  1989

4.  Lowe oculocerebrorenal syndrome: DNA-based linkage of the gene to Xq24-q26, using tightly linked flanking markers and the correlation to lens examination in carrier diagnosis.

Authors:  C Wadelius; P Fagerholm; U Pettersson; G Annerén
Journal:  Am J Hum Genet       Date:  1989-02       Impact factor: 11.025

Review 5.  Inherited metabolic diseases affecting the carrier.

Authors:  W Endres
Journal:  J Inherit Metab Dis       Date:  1997-03       Impact factor: 4.982

Review 6.  Cataract and metabolic disease.

Authors:  W Endres; Y S Shin
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

7.  [Clinical and genetic results with reference to corneal alterations in Lowe-syndrome].

Authors:  G Rudolph; P Kalpadakis; W Röschinger; C Haritoglou; S Kammerer; K-P Boergen; A Kampik
Journal:  Ophthalmologe       Date:  2004-06       Impact factor: 1.059

8.  Linkage studies in carriers of Lowe oculo-cerebro-renal syndrome.

Authors:  H M Hittner; A J Carroll; J T Prchal
Journal:  Am J Hum Genet       Date:  1982-11       Impact factor: 11.025

Review 9.  Lowe syndrome.

Authors:  Mario Loi
Journal:  Orphanet J Rare Dis       Date:  2006-05-18       Impact factor: 4.123

Review 10.  Lowe syndrome identified in the offspring of an oocyte donor who was an unknown carrier of a de novo mutation: a case report and review of the literature.

Authors:  P Tatsi; G E Papanikolaou; T Chartomatsidou; I Papoulidis; A Athanasiadis; R Najdecki; E Timotheou
Journal:  J Med Case Rep       Date:  2019-11-02
  10 in total

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