Literature DB >> 12654384

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

Carlo Incorvaia1, Francesco Parmeggiani, Ciro Costagliola, Paolo Perri, Marzia Tittoni, Adolfo Sebastiani.   

Abstract

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.

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Year:  2003        PMID: 12654384     DOI: 10.1016/s0002-9394(02)01979-7

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  1 in total

1.  Adrenal myelolipoma with keratoconus: A novel clinical association.

Authors:  Deep Dutta; Ks Shivaprasad; Sujoy Ghosh; Satinath Mukhopadhyay; Subhankar Chowdhury
Journal:  Indian J Endocrinol Metab       Date:  2012-12
  1 in total

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