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DOI 10.1136/bjo.81.8.639

Медицинская библиотека · The British journal of ophthalmology · 1997

Anterior segment dysgenesis in mosaic Turner syndrome.

Lloyd I C, Haigh P M, Clayton-Smith J, Clayton P, Price D A, Ridgway A E, Donnai D

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Аннотация

AIMS/

BACKGROUND

Females with Turner syndrome commonly exhibit ophthalmological abnormalities, although there is little information in the literature documenting findings specific to Turner syndrome mosaics. Ophthalmic findings are described in four patients with mosaic Turner syndrome. All had anterior chamber abnormalities and all four had karyotypic abnormalities with a 45, X cell line. The possible relation between the karyotypic and the phenotypic findings in these patients is discussed.

METHODS

Four girls with mosaic Turner syndrome underwent a full ophthalmological assessment, including examination under anaesthesia where indicated.

RESULTS

Three of the four patients presented with congenital glaucoma. Two had the karyotype 45, X/46, X, idic(Y) and one a 45, X/47, XXX karyotype. The remaining child had a Rieger malformation of the iris and the karyotype 45, X/46, X, r(X).

CONCLUSIONS

These findings suggest that Turner syndrome mosaicism (where there are two abnormal cell lines) is associated with anterior segment dysgenesis. The findings in these four patients are compared with those seen in other mosaic phenotypes and it is postulated that the presence of two or more genetically different cell lines may have an adverse effect on anterior segment development.

Для цитирования: Lloyd I C, Haigh P M, Clayton-Smith J, Clayton P, Price D A, Ridgway A E, Donnai D. Anterior segment dysgenesis in mosaic Turner syndrome.. The British journal of ophthalmology. 1997. DOI: 10.1136/bjo.81.8.639.

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