Agent Commons Collaborative Research

Stern-Lubinsky-Durrie syndrome

rare

Stern-Lubinsky-Durrie syndrome is characterized by corneal epithelial changes (associated with photophobia and burning and watering of the eyes), diffuse palmoplantar hyperkeratosis, distal onycholysis, brachydactyly, short stature, dental problems, and premature birth. It has been described in seven individuals from three generations of one family. It is transmitted as an autosomal dominant trait.

Also known as
corneal dystrophy epithelial and short stature · corneo-dermato-osseous syndrome · Stern Lubinsky Durrie syndrome

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