�ber seltene Duplikaturenbildungen in der embryonalen Netzhaut

Badtke, G.

doi:10.1007/bf00682436

Cited by 6 publications

(4 citation statements)

References 6 publications

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“…M ann explique la prédilection de cette m alform ation pour le q u ad ran t tem poral infé rieur, p ar une adhérence anorm ale du vitré prim aire à la face interne de la cupule optique, qui inhibe la form ation du vitré secondaire et provoque une traction sur les couches internes de la rétine, qui se plissent. Il est certain que la m alform ation a tte in t essentiellem ent le feuillet interne de la cupule optique prim itive qui s'hyperplasie (M ann, 1935 ;Badtke, 1954Badtke, , 1961) ( fig. 6 et 7).…”

Section: Histologieunclassified

Les malformations pseudotumorales du globe oculaire

Babel¹

1966

Ophthalmologica

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Section: Histologieunclassified

Les malformations pseudotumorales du globe oculaire

Babel¹

1966

Ophthalmologica

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“…This fact has been established, not only by Badtke (1954) but also by Weve (1935) and Joannid6s and Protonotarios (1965) in clinical observations, and by Ancona (1935) and Tillema (1937) in histopathological studies. This fact has been established, not only by Badtke (1954) but also by Weve (1935) and Joannid6s and Protonotarios (1965) in clinical observations, and by Ancona (1935) and Tillema (1937) in histopathological studies.…”

Section: Pathogenesis Of Congenital Retinal Foldmentioning

confidence: 71%

“…Apart from Weve's patients (1935Weve's patients ( , 1938 and the abovementioned cases, congenital retinal folds were reported in this quadrant by numerous other authors (Hoffman, 1926;Sttibel, 1927Sttibel, , 1928Tillema, 1937;Gartner, 1941;Theodore and Ziporkes, 1940;Poulsen, 1947;Van Manen, 1944;Von Winning, 1952;Badtke, 1954Badtke, , 1960Heydenreich, 1959;Joannid~s and Protonotarios, 1965;Thiel, 1968). Apart from Weve's patients (1935Weve's patients ( , 1938 and the abovementioned cases, congenital retinal folds were reported in this quadrant by numerous other authors (Hoffman, 1926;Sttibel, 1927Sttibel, , 1928Tillema, 1937;Gartner, 1941;Theodore and Ziporkes, 1940;Poulsen, 1947;Van Manen, 1944;Von Winning, 1952;Badtke, 1954Badtke, , 1960Heydenreich, 1959;Joannid~s and Protonotarios, 1965;Thiel, 1968).…”

Section: The Clinical Features Of Congenital Retinal Foldmentioning

confidence: 72%

“…Finally, the postulate that a falciform retinal fold results from an anomaly in the region of the embryonic ocular fissure (Pfliiger, 1885;Badtke, 1954Badtke, , 1960Palich-Sz~ntd, 1954) strikes me as hardly acceptable, because it is extremely rare to find the anomaly in the area where the embyronic optic cup closes, i.e. the inferior aspect of the eyeball, or even in the sector localized slightly nasal to it.…”

Section: 5a Early Versus Late Hypothesismentioning

confidence: 99%

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Dominant exudative vitreoretinopathy and other vascular developmental disorders of the peripheral retina

Nouhuys

1982

Doc Ophthalmol

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Developmental disorders of the retinal vasculature can be studied only in relation to the normal embryonic vascular development. Structural changes in the vasculature of the peripheral retina can be identified only by differentiating them from the normal vascular pattern. This is why this chapter discusses some aspects of the normal embryology and anatomy of the retinal vasculature which may be of importance for this study.

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Congenital retinal fold as a sign of dominant exudative vitreoretinopathy

1981

Albrecht von Graefes Arch. Klin. Ophthalmol.

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Four eyes of three patients from two large families with dominant exudative vitreoretinopathy showed an elevated retinal fold extending from the posterior pole toward the inferotemporal periphery of the fundus. A congenital retinal fold (ablatio falciformis congenita) has to be considered as a sign rather than a diagnosis, and can be caused by a few underlying disorders, to which dominant exudative vitreoretinopathy can be added. There are no indications that the hyaloid system is involved in the pathogenesis of a retinal fold in the latter condition. The formation of a retinal fold in dominant exudative vitreoretinopathy is the consequence of a developmental disorder of retinal vasculature during the last few months of intrauterine life, and may even occur after birth. The clinical picture and familial occurrence of many cases of congenital retinal fold described in the literature are suggestive of dominant exudative vitreoretinopathy, which only recently has been recognized as being a rather common condition.

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�ber seltene Duplikaturenbildungen in der embryonalen Netzhaut

Cited by 6 publications

References 6 publications

Les malformations pseudotumorales du globe oculaire

Les malformations pseudotumorales du globe oculaire

Dominant exudative vitreoretinopathy and other vascular developmental disorders of the peripheral retina

Congenital retinal fold as a sign of dominant exudative vitreoretinopathy

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