Corneodermatoosseous syndrome

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Corneodermatoosseous syndrom
Other namesCDO syndrome[1]
This condition is inherited in an autosomal dominant manner

Corneodermatosseous syndrome is an

diffuse palmoplantar keratoderma, distal onycholysis, skeletal abnormalities, with brachydactyly, short stature, and medullary narrowing of digits.[2]

See also

References

  1. ^ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Corneodermatoosseous syndrome". www.orpha.net. Retrieved 19 April 2019.{{cite web}}: CS1 maint: numeric names: authors list (link)
  2. .








External links