Pachyonychia congenita
Pachyonychia congenita is a rare hereditary skin disease of thick nails, first named by Jadassohn and Lewandowsky in 1906. Classification: It is usually divided into four types, type I is the most common, which is Jadassohn-Lewandowsky syndrome; type II is Jackson-Sertoli syndrome; type III is also known as Schaferer-Branauer syndrome; type IV is also known as late-onset congenital pachyonychia congenita tarda.
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Site of disease:
skin -
Infectious :
Not contagious -
Frequent population:
All groups -
Related symptoms:
Nail ingrown Hyperkeratosis of palm and plantar Cyst Follicular scaly keratosis Thickening of fingernails and toenails -
Concurrent disease:
Related Drugs
Children's diarrhea powder
Manufacturer:
Beijing Shunxin Xiangyun Pharmaceutical Co., Ltd.
Related Ingredients