BACKGROUND: Vohwinkel syndrome or keratoderma hereditaria mutilans is a rare autosomal dominant palmoplantar keratosis which manifests in infants and becomes more evident in adulthood. Patients with this mutation present hyperkeratosis of the palms and soles, constricting bands of the digits, usually at the fifth, and starfish-shaped hyperkeratosis on the dorsal aspects of the hands and feet. The disease mostly occurs in white women, where constricting fibrous bands appear on the digits and can lead to progressive strangulation and auto-amputation (pseudo-ainhum). AIM: The treatment of this keratoderma is very difficult and tends to be symptomatic: topical keratolytics and systemic retinoids have been used to treat hyperkeratosis, but with...
Keratoderma hereditarium mutilans (KHM) or Vohwinkel's syndrome is a rare cutaneous disorder, charac...
Abstract: Vohwinkel syndrome belongs to the group of hereditary palmoplantar keratoderma, having an ...
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...
Vohwinkel Syndrome, also known as Keratoderma Hereditarium Mutilans, is an extremely rare dominant a...
Vohwinkel syndrome or keratoderma hereditaria mutilans is a rare autosomal dominant palmoplantar ker...
Keratoderma hereditarium mutilans, or Vohwinkel syndrome, is a very rare genetic skin condition whic...
Keratoderma hereditarium mutilans, or Vohwinkel's syndrome, is a rare cutaneous disorder which is ch...
Vohwinkel syndrome belongs to the group of hereditary palmoplantar keratoderma, having an autosomal ...
A ceratodermia hereditária mutilante ou síndrome de Vohwinkel é afecção dermatológica rara caracteri...
A 28-year-old female born to consanguineous parents, presented with progressive palmoplantar kerato...
An 8-year-old girl with the classic findings of keraloderma heredilaria mutilans (Vohwinkel's syndro...
Abstract Vohwinkel’s syndrome is a rare, autosomal dominant disorder of keratinization characterized...
Pseudoainhum is a rare condition of unknown aetiology that is characterised by the presence of const...
Keratoderma hereditarium mutilans (KHM) or Vohwinkel's syndrome is a rare cutaneous disorder, charac...
Abstract: Vohwinkel syndrome belongs to the group of hereditary palmoplantar keratoderma, having an ...
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...
Vohwinkel Syndrome, also known as Keratoderma Hereditarium Mutilans, is an extremely rare dominant a...
Vohwinkel syndrome or keratoderma hereditaria mutilans is a rare autosomal dominant palmoplantar ker...
Keratoderma hereditarium mutilans, or Vohwinkel syndrome, is a very rare genetic skin condition whic...
Keratoderma hereditarium mutilans, or Vohwinkel's syndrome, is a rare cutaneous disorder which is ch...
Vohwinkel syndrome belongs to the group of hereditary palmoplantar keratoderma, having an autosomal ...
A ceratodermia hereditária mutilante ou síndrome de Vohwinkel é afecção dermatológica rara caracteri...
A 28-year-old female born to consanguineous parents, presented with progressive palmoplantar kerato...
An 8-year-old girl with the classic findings of keraloderma heredilaria mutilans (Vohwinkel's syndro...
Abstract Vohwinkel’s syndrome is a rare, autosomal dominant disorder of keratinization characterized...
Pseudoainhum is a rare condition of unknown aetiology that is characterised by the presence of const...
Keratoderma hereditarium mutilans (KHM) or Vohwinkel's syndrome is a rare cutaneous disorder, charac...
Abstract: Vohwinkel syndrome belongs to the group of hereditary palmoplantar keratoderma, having an ...
Mutilating palmoplantar keratoderma represents a heterogeneous group of disorders, unified by charac...