EDICT syndrome
Synonyms: Autosomal dominant keratoconus with early-onset anterior polar cataracts | Endothelial dystrophy-iris hypoplasia-congenital cataract-stromal thinning syndrome | Familial keratoconus with cataract | KTCNCT
A rare autosomal dominant eye disorder representing a constellation of inherited ocular findings including early-onset or congenital cataracts corneal stromal thinning early-onset keratoconus corneal endothelial dystrophy and iris hypoplasia.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024
Newly diagnosed with
EDICT syndrome?
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Advocacy Organizations
Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
Clinical Trials
For a list of clinical trials in this disease area, please click here.