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American journal of ophthalmology · 2003

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency associated with bilateral keratoconus.

Клинический случайСтатьяНазвание и аннотация: Перевод пока не подготовлен
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Incorvaia Carlo, Parmeggiani Francesco, Costagliola Ciro, Perri Paolo, Tittoni Marzia, Sebastiani Adolfo

Аннотация

PURPOSE: To report a clinical association between congenital adrenal hyperplasia and keratoconus.

DESIGN: Observational case report.

METHODS: Two 25-year-old dizygotic female twins were retrospectively studied. Clinical history, hormonal serologic profile, complete ophthalmologic examination, and Holladay Diagnostic Summary variables were evaluated. In the course of a 15-month follow-up period, a progression of the corneal disease was observed.

RESULTS: In both twins a diagnosis of nonclassical congenital adrenal hyperplasia, due to 21-hydroxylase deficiency, was established when they were 21 years old. In one subject, the computed corneal topographic analyses diagnosed an asymmetric keratoconus in both eyes. A progressive form of fruste central keratoconus was also documented in her sister.

CONCLUSIONS: Congenital adrenal hyperplasia may be associated with keratoconus. An abnormal steroidogenic pathway, affecting the normal development of the cornea, could induce stromal abnormalities that lead to corneal ectasia.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты