Hereditary progressive arthro-ophthalmopathy of Stickler

Norman P. Blair, Daniel Albert, Ruth M. Liberfarb, Tatsuo Hirose

Research output: Contribution to journalArticle

43 Citations (Scopus)

Abstract

The ocular histopathologic findings in three patients with the Stickler syndrome from two families included the following: total retinal detachment with marked folding, disorganization of the retina, and a preretinal membrane. The progression of the fundus lesions was followed up in two patients during the course of 30 and 24 years. Many cases variously reported as Wagner's disease, familial retinal detachment, hyaloideoretinopathy with cleft palate, and the Pierre Robin syndrome probably were the Stickler syndrome.

Original languageEnglish (US)
Pages (from-to)876-888
Number of pages13
JournalAmerican journal of ophthalmology
Volume88
Issue number5
DOIs
StatePublished - Jan 1 1979
Externally publishedYes

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Retinal Detachment
Pierre Robin Syndrome
Cleft Palate
Retina
Membranes
Type 1 Stickler syndrome
Hyaloideoretinal degeneration of Wagner

ASJC Scopus subject areas

  • Ophthalmology

Cite this

Hereditary progressive arthro-ophthalmopathy of Stickler. / Blair, Norman P.; Albert, Daniel; Liberfarb, Ruth M.; Hirose, Tatsuo.

In: American journal of ophthalmology, Vol. 88, No. 5, 01.01.1979, p. 876-888.

Research output: Contribution to journalArticle

Blair, Norman P. ; Albert, Daniel ; Liberfarb, Ruth M. ; Hirose, Tatsuo. / Hereditary progressive arthro-ophthalmopathy of Stickler. In: American journal of ophthalmology. 1979 ; Vol. 88, No. 5. pp. 876-888.
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