Related MeSH Hierarchy (5)
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Skin Abnormalities » Ectodermal Dysplasia » Pachyonychia Congenita » Steatocystoma Multiplex
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Skin Diseases, Genetic » Ectodermal Dysplasia » Pachyonychia Congenita » Steatocystoma Multiplex
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Nail Diseases » Pachyonychia Congenita » Steatocystoma Multiplex
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Abnormalities » Ectodermal Dysplasia » Pachyonychia Congenita » Steatocystoma Multiplex
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Genetic » Ectodermal Dysplasia » Pachyonychia Congenita » Steatocystoma Multiplex
Description
A disorder characterized by multiple, wide spread cutaneous cysts that often become inflamed and rupture. It is caused by the same mutations in the gene coding for KRT-17 that are causative mutations for Pachyonychia congenita, Type 2. Natal teeth involvement is sometimes associated with steatocystoma multiplex. MeSH
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