Dental diseases, skin changes

Due to the joint development from the ectoderm, diseases of the teeth and the skin can occur in close connection. These include genetic, infectious and non-infectious inflammatory and immunologically accentuated diseases. Thus, some systemic diseases in their syndromal complexity only reveal themselves in an overall view (and recording) of their symptoms. Thus, the assessment of dental diseases is also part of the scope of a comprehensive, subtle dermatological diagnosis.

In the following, very heterogeneous diseases are listed in which skin and teeth are equally affected. In detail these include:

• Hyper-IgE Syndrome
• Leukocyte adhesion-deficiency syndrome (severe periodontitis possibly with tooth loss)
• Syphilis connata (see also Hutchinson teeth)
• Ectodermal Dysplasia - Group
• Epidermolysis bullosa group
• Gardner syndrome I
• Goltz-Gorlin Syndrome
• Langerhans cell histiocytosis
• Bourneville-Pringle Syndrome
• Rabson-Mendenhall Syndrome
• Incontinentia pigmenti achromians (Hypomelanosis Ito)
• incontinentia pigmenti
• Incontinentia pigmenti, type Franceschetti-Jadassohn-Naegeli
• Chediak Higashi Syndrome
• Congenital erythropoietic porphyria
• Papillon-Lefèvre syndrome
• Sjögren-Larsson Syndrome
• Hystrix-like Ithyosis Deafness Syndrome
• Zunich-Kaye Syndrome
• Progeria
• Ehlers-Danlos Syndrome
• Kindler Syndrome
• hypertrichosis lanuginosa congenita
• Okulo-fazio-cardio-dental syndrome.