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Naegeli–Franceschetti–Jadassohn syndrome: A rare case
Naegeli–Franceschetti–Jadassohn Syndrome (NFJS) is a rare, autosomal dominant inherited form of ectodermal dysplasia, caused by mutation in the KRT14 gene. We report here a case of NFJS in a 27-year-old male who presented with reticulate hyperpigmentation over skin, dental changes, absence of dermat...
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| Udgivet i: | Indian Dermatol Online J |
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| Main Authors: | , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Medknow Publications & Media Pvt Ltd
2015
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4693352/ https://ncbi.nlm.nih.gov/pubmed/26753140 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2229-5178.169712 |
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