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Focal Dermal Hypoplasia (Syndrome, Goltz) Summary

Description: A genetic skin disease characterized by hypoplasia of the dermis, herniations of fat, and hand anomalies. It is found exclusively in females and transmitted as an X-linked dominant trait.

Also Known As: Syndrome, Goltz; Goltz's Syndrome; Goltz-Gorlin Syndrome; Dermal Hypoplasias, Focal; Focal Dermal Hypoplasias Show All >>

Networked: 44 relevant articles (0 outcomes, 0 trials/studies) for this Disease

Key Drugs and Agents for Focal Dermal Hypoplasia

Efficacy Chart >>
Drugs and Important Biological Agents (IBA) related to treatments:
  1. syndromic 7 Microphthalmia : 7 results : IBA
  2. Oculocerebrocutaneous syndrome : 4 results : IBA
  3. Ectrodactyly : 4 results : IBA
  4. Mesoectodermal dysplasia : 3 results : IBA
  5. Hypohidrotic Ectodermal Dysplasia : 3 results : IBA
  6. Encephalocraniocutaneous lipomatosis : 3 results : IBA
  7. Wnt Proteins : 2 results : IBA
  8. Nonsense Codon (Nonsense Mutation) : 2 results : IBA
  9. Valproic acid antenatal infection : 2 results : IBA
  10. Ectrodactyly-cleft lip/palate syndrome : 2 results : IBA
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Diseases Related to Focal Dermal Hypoplasia

  1. Focal Dermal Hypoplasia (Syndrome, Goltz)
  2. Pentalogy of Cantrell
  3. Incontinentia Pigmenti (Bloch Sulzberger Syndrome)
  4. Umbilical Hernia (Omphalocele)
  5. Ectodermal Dysplasia (Aplasia Cutis Congenita)
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Key Therapies for Focal Dermal Hypoplasia

Efficacy Chart >>
  1. Photochemotherapy (Photodynamic Therapy) : 2 results
  2. Airway Management : 1 result
  3. Dental Care : 1 result
  4. Curettage : 1 result
  5. Bone Nails : 1 result
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