Corneodermatoosseous syndrome

Corneodermatosseous syndrome is an autosomal dominant condition with onset in infancy, characterized by corneal dystrophy, photophobia, diffuse palmoplantar keratoderma, distal onycholysis, skeletal abnormalities, with brachydactyly, short stature, and medullary narrowing of digits.^[2]

Corneodermatoosseous syndrom
Other names	CDO syndrome[1]
This condition is inherited in an autosomal dominant manner
Specialty	Medical genetics

See also

• Palmoplantar keratoderma
• Keratoderma
• Skin lesion
• Terminal osseous dysplasia with pigmentary defects
• List of cutaneous conditions