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of or relating to mucous membranes

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世襲の,親譲りの / 遺伝的な,遺伝性の

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1. 化学療法に関連した経口毒性 oral toxicity associated with chemotherapy
2. アフタ性口内炎、咽頭炎およびリンパ節炎（PFAPA症候群）を伴う周期熱 periodic fever with aphthous stomatitis pharyngitis and adenitis pfapa syndrome
3. 癌性疼痛症候群の概要 overview of cancer pain syndromes
4. 若齢小児におけるヘルペス性歯肉口内炎 herpetic gingivostomatitis in young children
5. 頭頸部癌の初期治療中の合併症のマネージメントおよび予防 management and prevention of complications during initial treatment of head and neck cancer

English Journal

Expression profiling of white sponge nevus by RNA sequencing revealed pathological pathways.

Cai W1, Jiang B2, Feng T3, Xue J4, Yang J5, Chen Z6, Liu J7, Wei R7, Zhao S8, Wang X9, Liu S10.
Orphanet journal of rare diseases.Orphanet J Rare Dis.2015 Jun 11;10:72. doi: 10.1186/s13023-015-0285-y.
BACKGROUND: White sponge nevus (WSN) is a rare periodontal hereditary disease. To date, almost all WSN studies have focused on case reports or mutation reports. Thus, the mechanism behind WSN is still unclear. We investigated the pathogenesis of WSN using expression profiling.METHODS: Sequence analy
PMID 26062705

Current approaches to the diagnosis and treatment of white sponge nevus.

Cai W1, Jiang B2, Yu F2, Yang J3, Chen Z3, Liu J3, Wei R3, Zhao S1, Wang X2, Liu S1.
Expert reviews in molecular medicine.Expert Rev Mol Med.2015 May 29;17:e9. doi: 10.1017/erm.2015.7.
White sponge nevus (WSN) in the oral mucosa is a rare autosomal dominant genetic disease. The involved mucosa is white or greyish, thickened, folded and spongy. The genes associated with WSN include mutant cytokeratin keratin 4 (KRT4) and keratin 13 (KRT13). In recent years, new cases of WSN and ass
PMID 26021387

White sponge nevus - a rare autosomal dominant keratinopathy.

Benoit S1, Schlipf N2, Hausser I3, Fischer J2, Hamm H1.
Klinische Pädiatrie.Klin Padiatr.2014 Nov;226(6-7):375-6. doi: 10.1055/s-0034-1371843. Epub 2014 May 8.
PMID 24810752

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