Zum Krankheitsbild der familiären Tortuositas der kleinen Netzhautgefäße

Cagianut, B.

doi:10.1159/000305472

Cited by 10 publications

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“…In the present case onset and course of the disease were like those ofthe earlier reported cases of spontaneous retinal haemorrhages with arteriolar tortuosity [1][2][3][4][5][6][7], A basic dis ease has not been found in any of these cases.…”

Section: Discussionsupporting

confidence: 86%

Retinal Vascular Tortuosity and Recurrent Retinal Haemorrhages in a Patient with Non-Chromaffin Paraganglioma

1985

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Section: Discussionsupporting

confidence: 86%

Retinal Vascular Tortuosity and Recurrent Retinal Haemorrhages in a Patient with Non-Chromaffin Paraganglioma

1985

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“…T h e combination of retinal arteriolar tortuosity with spontaneous retinal haemorrhages seems to be a rare clinical picture unnoticed until it was reported from East-Germany by Beyer (1958). Later similar cases have been reported from Switzerland (Cagianut 1968; Cagianut & Werner 1968), North America (Goldberg et al 1972) andWest-Germany (Stefani et al 1975). T h e condition has not previously been reported in Scandinavia.…”

mentioning

confidence: 54%

Retinal Arteriolar Tortuosity With Retinal Haemorrhage

Olsen

1978

Acta Ophthalmologica

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Retinal arteriolar tortuosity with retinal haemorrhages was first described in 1958. In the present article, a case of recurring retinal haemorrhages combined with retinal arteriolar tortuosity is reported. The medical examination and laboratory tests did not reveal pathology except for a slightly increased bleeding time. There were no similar cases in the family. The cause of the haemorrhages is still unknown.

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“…The father had hypogammaglobulinaemia, which may be of some interest as retinal microaneurysms were reported by Frenkel & Russe (1967) in a patient with hypogammaglobulinaemia. Cagianut & Werner (1968) reported four patients from a family with retinal arteriolar tortuosity and recurrent haemorrhages. Venules were normal.…”

Section: Discussionmentioning

confidence: 99%

Hereditary Central Retinal Angiopathy

Ehlers¹,

Jensen²

1973

Acta Ophthalmologica

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A family, with three members affected by a central retinal angiopathy, is reported. The fundus changes consisted of tortuous arterioles, ectatic capillaries, microaneurysms, small retinal haemorrhages and tiny white dots. The changes were demonstrated by colour fluorescein angiography. The retinal changes simulate those described in hereditary haemorrhagic teleangiectasia (Rendu-Osler-Weber's disease) and in familial retinal arteriolar tortuosity, both showing dominant inheritance. Although none of the three patients had other stigmata of hereditary haemorrhagic teleangiectasia, it is proposed to consider the presently reported cases, as well as those reported under the diagnosis of familial arteriolar tortuosity, as a localized manifestation of a disorder which in other families may give the clinical picture of Rendu-Osler-Weber's disease.

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Zum Krankheitsbild der familiären Tortuositas der kleinen Netzhautgefäße

Cited by 10 publications

References 0 publications

Retinal Vascular Tortuosity and Recurrent Retinal Haemorrhages in a Patient with Non-Chromaffin Paraganglioma

Retinal Vascular Tortuosity and Recurrent Retinal Haemorrhages in a Patient with Non-Chromaffin Paraganglioma

Retinal Arteriolar Tortuosity With Retinal Haemorrhage

Hereditary Central Retinal Angiopathy

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