A 28-year-old female born to consanguineous parents, presented with progressive palmoplantar keratoderma since the age of six months and a constricting band on right fourth finger of one year duration. There was history of similar complaints being present in two other family members. Associated clinical findings included starfish-shaped cornified plaques on knuckles, resorption of distal phalanges and keratotic plaques on elbows, groins and knees. The patient was mentally sound and had normal audiometry. Biopsy from hyperkeratotic plaque showed hyperkeratosis, parakeratosis, increased granular layer and papillomatosis. Gene mapping for loricrin mutation was found to be negative
Vohwinkel Syndrome, also known as Keratoderma Hereditarium Mutilans, is an extremely rare dominant a...
Loricrin keratoderma is an autosomal dominant palmoplantar keratoderma heterogeneous in clinical app...
BACKGROUND We describe a male with functionally impairing radial deviation of the thumb who presente...
Vohwinkel syndrome or keratoderma hereditaria mutilans is a rare autosomal dominant palmoplantar ker...
Abstract Vohwinkel’s syndrome is a rare, autosomal dominant disorder of keratinization characterized...
Abstract: Vohwinkel syndrome belongs to the group of hereditary palmoplantar keratoderma, having an ...
Vohwinkel syndrome belongs to the group of hereditary palmoplantar keratoderma, having an autosomal ...
Keratoderma hereditarium mutilans, or Vohwinkel's syndrome, is a rare cutaneous disorder which is ch...
Mutilating palmoplantar keratoderma represents a heterogeneous group of disorders, unified by charac...
BACKGROUND: Vohwinkel syndrome or keratoderma hereditaria mutilans is a rare autosomal dominant palm...
BACKGROUND: Vohwinkel syndrome or keratoderma hereditaria mutilans is a rare autosomal dominant palm...
We describe a female patient with Vohwinkel syndrome (mutilating palmoplantar keratoderma), who in a...
Keratoderma hereditarium mutilans, or Vohwinkel syndrome, is a very rare genetic skin condition whic...
Keratoderma hereditarium mutilans (KHM) or Vohwinkel's syndrome is a rare cutaneous disorder, charac...
A mutation in the gene encoding loricrin has recently been reported in a subset of patients with Voh...
Vohwinkel Syndrome, also known as Keratoderma Hereditarium Mutilans, is an extremely rare dominant a...
Loricrin keratoderma is an autosomal dominant palmoplantar keratoderma heterogeneous in clinical app...
BACKGROUND We describe a male with functionally impairing radial deviation of the thumb who presente...
Vohwinkel syndrome or keratoderma hereditaria mutilans is a rare autosomal dominant palmoplantar ker...
Abstract Vohwinkel’s syndrome is a rare, autosomal dominant disorder of keratinization characterized...
Abstract: Vohwinkel syndrome belongs to the group of hereditary palmoplantar keratoderma, having an ...
Vohwinkel syndrome belongs to the group of hereditary palmoplantar keratoderma, having an autosomal ...
Keratoderma hereditarium mutilans, or Vohwinkel's syndrome, is a rare cutaneous disorder which is ch...
Mutilating palmoplantar keratoderma represents a heterogeneous group of disorders, unified by charac...
BACKGROUND: Vohwinkel syndrome or keratoderma hereditaria mutilans is a rare autosomal dominant palm...
BACKGROUND: Vohwinkel syndrome or keratoderma hereditaria mutilans is a rare autosomal dominant palm...
We describe a female patient with Vohwinkel syndrome (mutilating palmoplantar keratoderma), who in a...
Keratoderma hereditarium mutilans, or Vohwinkel syndrome, is a very rare genetic skin condition whic...
Keratoderma hereditarium mutilans (KHM) or Vohwinkel's syndrome is a rare cutaneous disorder, charac...
A mutation in the gene encoding loricrin has recently been reported in a subset of patients with Voh...
Vohwinkel Syndrome, also known as Keratoderma Hereditarium Mutilans, is an extremely rare dominant a...
Loricrin keratoderma is an autosomal dominant palmoplantar keratoderma heterogeneous in clinical app...
BACKGROUND We describe a male with functionally impairing radial deviation of the thumb who presente...
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