Literature DB >> 27169914

A family with sex linked optic atrophy : Ophthalmological and neurological aspects.

H J Völker-Dieben1, G H Van Lith2, L N Went3, J W Klawer4, A Staal4, E C De Vries-De Mol3.   

Abstract

A large family in which 8 males are affected with apparently sex linked optic atrophy is described. The disease has been present since early childhood, and the visual acuity ranges between 1/60 and 0.4. The fundi are very typical: pale optic discs, frequently with cupping and an abnormal vascularity. In all cases visual fields are normal on the periphery with somewhat enlarged blind spots or paracentral scotomata in the older patients.All patients were investigated electro-ophthalmologically. The clearly abnormal VECPs and the very probably normal ERG in the youngest patient indicate that the disturbance in the conductive system is prior to that of the retina. Fluorescence angiography revealed the typical appearance of optic atrophy.In addition to the typical findings of the optic atrophy also neurological abnormalities varying between very mild to more severe were observed in the patients. Neurological examination revealed definitely abnormalities but classification was not possible. Symptoms of Huntington's Chorea were not found.Ophthalmological, electro-ophthalmolocigal, fluorescein-angiographic and neurological studies in the female carriers did not reveal any abnormalities.An analysis of all other types of optic atrophy described hitherto in the literature did not reveal comparable cases to the ones seen in our family.

Entities:  

Year:  1974        PMID: 27169914     DOI: 10.1007/BF00147264

Source DB:  PubMed          Journal:  Doc Ophthalmol        ISSN: 0012-4486            Impact factor:   2.379


  11 in total

Review 1.  LEBER'S DISEASE IN THE NETHERLANDS.

Authors:  A H VANSENUS
Journal:  Doc Ophthalmol       Date:  1963       Impact factor: 2.379

2.  FLUORESCEIN PHOTOGRAPHY OF THE OCULAR FUNDUS.

Authors:  J A OOSTERHUIS; A J LAMMENS
Journal:  Ophthalmologica       Date:  1965       Impact factor: 3.250

3.  Ophthalmoplegia and retinal degeneration associated with spinocerebellar ataxia.

Authors:  R S JAMPEL; H OKAZAKI; H BERNSTEIN
Journal:  Arch Ophthalmol       Date:  1961-08

4.  A sex-linked recessive form of spastic paraplegia.

Authors:  A W JOHNSTON; V A McKUSICK
Journal:  Am J Hum Genet       Date:  1962-03       Impact factor: 11.025

5.  Retinal degeneration in hereditary ataxia.

Authors:  A BJORK; U LINDBLOM; L WADENSTEN
Journal:  J Neurol Neurosurg Psychiatry       Date:  1956-08       Impact factor: 10.154

6.  Similarities between congenital tritan defects and dominant optic-nerve atrophy: coincidence or identity?

Authors:  A E Krill; V C Smith; J Pokorny
Journal:  J Opt Soc Am       Date:  1970-08

7.  Four families with the dominant infantile form of optic nerve atrophy.

Authors:  C C Kok-van Alphen
Journal:  Acta Ophthalmol (Copenh)       Date:  1970

8.  [On electroretinographic findings in cases of dominant juvenile optic atrophy].

Authors:  K A Hellner; W Haase
Journal:  Albrecht Von Graefes Arch Klin Exp Ophthalmol       Date:  1967

9.  Hereditary optic atrophy. An autosomal dominant with incomplete penetrance.

Authors:  L R Shapiro; E L Raab; I H Leopold; K Hirschhorn
Journal:  Arch Ophthalmol       Date:  1969-03

10.  Two kindreds with a sex-linked recessive form of spastic paraplegia.

Authors:  T F Thurmon; B A Walker; C I Scott; M H Abbott
Journal:  Birth Defects Orig Artic Ser       Date:  1971-02
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  2 in total

1.  X-recessive angiopathic opticopathy.

Authors:  L A Bastiaensen; J J Vandoninck
Journal:  Doc Ophthalmol       Date:  1982-01-29       Impact factor: 2.379

Review 2.  A review of primary hereditary optic neuropathies.

Authors:  M Votruba; S Aijaz; A T Moore
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

  2 in total

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