Angioid streaks associated with abetalipoproteinemia.

J. P. Dieckert; M. White; L. Christmann; H. M. Lambert

Angioid streaks associated with abetalipoproteinemia.

J. P. Dieckert, M. White, L. Christmann, H. M. Lambert

Research output: Contribution to journal › Article › peer-review

Abstract

Angioid streaks were observed in a 31-year-old man with abetalipoproteinemia. Angioid streaks have now been described in hereditary spherocytosis, beta thalassemia, alpha thalassemia, sickle cell anemia, and acanthocytosis secondary to abetalipoproteinemia and hypobetalipoproteinemia. The nature of the association of angioid streaks and structural defects of hemoglobin and the red blood cell is not understood.

Original language	English (US)
Pages (from-to)	173-175, 179
Journal	Annals of Ophthalmology
Volume	21
Issue number	5
State	Published - May 1989

ASJC Scopus subject areas

Ophthalmology

Cite this

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title = "Angioid streaks associated with abetalipoproteinemia.",

abstract = "Angioid streaks were observed in a 31-year-old man with abetalipoproteinemia. Angioid streaks have now been described in hereditary spherocytosis, beta thalassemia, alpha thalassemia, sickle cell anemia, and acanthocytosis secondary to abetalipoproteinemia and hypobetalipoproteinemia. The nature of the association of angioid streaks and structural defects of hemoglobin and the red blood cell is not understood.",

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AU - Dieckert, J. P.

AU - White, M.

AU - Christmann, L.

AU - Lambert, H. M.

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N2 - Angioid streaks were observed in a 31-year-old man with abetalipoproteinemia. Angioid streaks have now been described in hereditary spherocytosis, beta thalassemia, alpha thalassemia, sickle cell anemia, and acanthocytosis secondary to abetalipoproteinemia and hypobetalipoproteinemia. The nature of the association of angioid streaks and structural defects of hemoglobin and the red blood cell is not understood.

AB - Angioid streaks were observed in a 31-year-old man with abetalipoproteinemia. Angioid streaks have now been described in hereditary spherocytosis, beta thalassemia, alpha thalassemia, sickle cell anemia, and acanthocytosis secondary to abetalipoproteinemia and hypobetalipoproteinemia. The nature of the association of angioid streaks and structural defects of hemoglobin and the red blood cell is not understood.

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ER -

Angioid streaks associated with abetalipoproteinemia.

Abstract

ASJC Scopus subject areas

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