Eine recessiv-geschlechtsgebundene Form der idiopathischen Netzhautspaltung bei nichtmyopen Jugendlichen

Kleinert, H

doi:10.1007/bf00682091

Cited by 14 publications

(4 citation statements)

References 10 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…The macular area of the fundus is slightly elevated and an optically almost empty zone separates two retinal layers of which the superficial very thin one shows a typical radiate folding. This finding was beautifully described by Jager (1953) and Kleinert (1953). All cases in our material had this lesion on both eyes.…”

Section: Discussionsupporting

confidence: 90%

See 1 more Smart Citation

Sex‐linked Hereditary Juvenile Retinoschisis

Bengtsson

Linder

1967

Acta Ophthalmologica

View full text Add to dashboard Cite

Section: Discussionsupporting

confidence: 90%

“…Haemorrhages in the retinn and the vitreous are not unusual, as described by Juler (1948 and 1951). Magnus (1951), Sheehan (1952), Kleinert (1953) and Ricci (1961). In our family I no case with bleeding was found at the examination, but one in family I1 (IV:2) had had several retinal bleedings.…”

Section: Discussionmentioning

confidence: 55%

Sex‐linked Hereditary Juvenile Retinoschisis

Bengtsson

Linder

1967

Acta Ophthalmologica

View full text Add to dashboard Cite

“…Nineteen years had elapsed since the first investigation. Kleinert (1953) studied an eye which had been described 19 years earlier. The macular area showed relatively slight progression of the disease, the only evidence being thickening of the radia!…”

mentioning

confidence: 99%

Progression in juvenile X‐chromosomal retinoschisis

Forsius¹,

Eriksson²,

Damsten³

1990

Acta Ophthalmologica

View full text Add to dashboard Cite

Forty-five males and one homozygotic female showing X-chromosomal juvenile retinoschisis were re-investigated in 1987 after an average follow-up study of more than 22 years. Twenty-two of them had been investigated by fundus-photography for at least 14 years.With time, the typical radial micro-cystic macular area flattens out and atrophies. In very old persons only some large choroidal vessels are seen, covering the sclera in the previously radiating area. In young patients with additional peripheral schisis the veil ruptures, the schisis area flattens out, the holes grow and may unite. In the outer retinal layer pigment degeneration develops. In congenitally severe cases the atrophy is marked and rapid. The retinal vessels attenuate and the nerve head becomes pale. Total blindness results in cases of this cathegory. The severity of retinoschisis varies much in patients belonging to the same family and even in the two eyes of the same person.

show abstract

“…Only one case has been observed in a female homozygote (Forsius et al 1963). Important contributions to the syndrome have been given by Kleinert (1953), ]uger (1953), and Gieser & Falls (1961).…”

mentioning

confidence: 99%

Hereditary Hyaloideo‐retinal Degeneration (Wagner) in a Danish Family

Frandsen

1966

Acta Ophthalmologica

View full text Add to dashboard Cite

Eine recessiv-geschlechtsgebundene Form der idiopathischen Netzhautspaltung bei nichtmyopen Jugendlichen

Cited by 14 publications

References 10 publications

Sex‐linked Hereditary Juvenile Retinoschisis

Sex‐linked Hereditary Juvenile Retinoschisis

Progression in juvenile X‐chromosomal retinoschisis

Hereditary Hyaloideo‐retinal Degeneration (Wagner) in a Danish Family

Contact Info

Product

Resources

About