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Vohwinkel Syndrome, Variant Form

Known as: LORICRIN KERATODERMA, MUTILATING KERATODERMA WITH ICHTHYOSIS, Vohwinkel Syndrome with Ichthyosis 
National Institutes of Health

Related topics

Related topics

4 relations
Autosomal dominant inheritanceHyperkeratosisParakeratosis

Broader (1)

Skin Diseases, Genetic

Papers overview

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1999
1999
Loricrin Keratoderma:免疫電顕による病因と病態の解明 (特集 免疫電顕で皮膚病に迫る)
1984
1984
[Contribution to our knowledge of Thévenard's ulcero-mutilating acropathy].
Four patients presenting ulcerative mutilating acropathy (UMA) (Thévenard's disease or Denny-Brown's hereditary sensory… 
1977
1977
[A sporadic form of ulcero-mutilating acropathy].
1966
1966
[A sporadic case of the pareto-amyotrophic form of ulcero-mutilating acropathy].
1966
1966
[Polyneuritic paramyloidosis of the Portuguese type (familial amyloid polyneuropathy). A differential diagnosis from ulcero-mutilating acropathy].