Corneodermatosseous syndrome is an
autosomal dominant
In genetics, dominance is the phenomenon of one variant (allele) of a gene on a chromosome masking or overriding the effect of a different variant of the same gene on the other copy of the chromosome. The first variant is termed dominant and t ...
condition with onset in infancy, characterized by corneal dystrophy, photophobia,
diffuse palmoplantar keratoderma
Palmoplantar keratodermas are a heterogeneous group of disorders characterized by abnormal thickening of the stratum corneum of the palms and soles.
Autosomal recessive, dominant trait, dominant, X-linked, and acquired forms have all been describe ...
, distal onycholysis, skeletal abnormalities, with brachydactyly, short stature, and medullary narrowing of digits.
See also
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Palmoplantar keratoderma
Palmoplantar keratodermas are a heterogeneous group of disorders characterized by abnormal thickening of the stratum corneum of the palms and soles.
Autosomal recessive, dominant, X-linked, and acquired forms have all been described.
Types
Cli ...
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Keratoderma
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Skin lesion
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Terminal osseous dysplasia with pigmentary defects
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List of cutaneous conditions
Many skin conditions affect the human integumentary system—the organ system covering the entire surface of the body and composed of skin, hair, nails, and related muscle and glands. The major function of this system is as a barrier against t ...
References
External links
Palmoplantar keratodermas
Syndromes affecting the cornea
Syndromes with short stature
Syndromes with dysmelia
{{Cutaneous-condition-stub