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Oral Findings of Rothmund-Thomson Syndrome
Rothmund-Thomson syndrome (RTS) is an extremely rare genetic condition exhibiting some dermatological, craniofacial, ophthalmological, and central nervous system abnormalities. It has an autosomal, recessive inheritance and its signs begin at childhood. Essential dermatological alteration is poikilo...
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| Hlavní autoři: | , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Hindawi Publishing Corporation
2013
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| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3864084/ https://ncbi.nlm.nih.gov/pubmed/24363941 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2013/935716 |
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