Vohwinkel syndrome

Deafness, congenital, with keratopachydermia and constrictions of fingers and toes

Also Known As:

Keratoderma hereditarium mutilans; Mutilating keratoderma

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 668
- Congenital Abnormalities: 15467
  - Multiple Abnormalities: 163
    - Vohwinkel syndrome: 33
  - Musculoskeletal Abnormalities: 36
    - Congenital Limb Deformities: 7
      - Congenital Hand Deformities: 4
        Vohwinkel syndrome: 33
- Inborn Genetic Diseases: 842
  - Genetic Skin Diseases: 21
    - Palmoplantar Keratoderma: 281
      - Vohwinkel syndrome: 33
Musculoskeletal Diseases: 179
- Hand Deformities: 43
  - Congenital Hand Deformities: 4
    - Vohwinkel syndrome: 33
- Musculoskeletal Abnormalities: 36
  - Congenital Limb Deformities: 7
    - Congenital Upper Extremity Deformities
      - Congenital Hand Deformities: 4
        Vohwinkel syndrome: 33
Otorhinolaryngologic Diseases: 130
- Ear Diseases: 150
  - Hearing Disorders: 223
    - Hearing Loss: 6504
      - Sensorineural Hearing Loss: 2162
        Vohwinkel syndrome: 33
Nervous System Diseases: 6158
- Neurologic Manifestations: 4205
  - Sensation Disorders: 69
    - Hearing Disorders: 223
      - Hearing Loss: 6504
        Sensorineural Hearing Loss: 2162
        Vohwinkel syndrome: 33
Signs and Symptoms Pathological Conditions
- Signs and Symptoms
  - Neurologic Manifestations: 4205
    - Sensation Disorders: 69
      - Hearing Disorders: 223
        Hearing Loss: 6504
        Sensorineural Hearing Loss: 2162
        Vohwinkel syndrome: 33
Skin and Connective Tissue Diseases
- Skin Diseases: 8226
  - Keratosis: 577
    - Palmoplantar Keratoderma: 281
      - Vohwinkel syndrome: 33
  - Genetic Skin Diseases: 21
    - Palmoplantar Keratoderma: 281
      - Vohwinkel syndrome: 33

Rossella Sferrazza Selected Research

Rossella Sferrazza Research Topics

Disease

Drug/Important Bio-Agent (IBA)

Therapy/Procedure