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1. 成人に生じる全身性硬化症（全身性強皮症）の臨床症状と診断clinical manifestations and diagnosis of systemic sclerosis scleroderma in adults [show details]
… alterations, or renal failure consistent with scleroderma renal crisis (SRC) Early referral to a rheumatologist is recommended when SSc sine scleroderma is suspected in order to avoid delay in diagnosis …
2. 皮膚剥脱症候群peeling skin syndromes [show details]
… all coding regions of the TGM5 gene is indicated. Generalized noninflammatory peeling skin syndrome (PSS), or type A PSS (MIM #270300), is a rare, autosomal recessive disorder characterized by generalized …
3. 強皮症腎クリーゼを含む全身性硬化症（強皮症）における腎疾患renal disease in systemic sclerosis scleroderma including scleroderma renal crisis [show details]
… of SSc, but lack the characteristic skin changes, a disease subset called systemic sclerosis sine scleroderma . In this setting, other signs of SSc should be sought. These include: Digital tip pitting …
4. 成人における全身性硬化症（強皮症）の治療および予後の概要overview of the treatment and prognosis of systemic sclerosis scleroderma in adults [show details]
…percent of patients have internal organ involvement without skin involvement, referred to as SSc sine scleroderma. These patients are generally managed in a way similar to those classified as having the limited …
5. 全身性硬化症（強皮症）の成人の前治療評価pretreatment evaluation of adults with systemic sclerosis scleroderma [show details]
… cutaneous systemic sclerosis (dcSSc) Limited cutaneous systemic sclerosis (lcSSc) Systemic sclerosis sine scleroderma (patients with only internal organ involvement) Overlap syndromes (features of systemic sclerosis …

English Journal

Progressive systemic sclerosis sine scleroderma which developed after exposure to epoxy resin polymerization.

Inachi S, Mizutani H, Ando Y, Shimizu M.
The Journal of dermatology. 1996 May;23(5)344-6.
Progressive systemic sclerosis (PSS) sine scleroderma is well known as a special form of scleroderma. Because of its rarity, its pathogenesis has not yet been elucidated. We experienced a 33-year-old man who developed PSS sine scleroderma while working with epoxy resin polymerization. He had short w
PMID 8675826

[Telangiectasias in progressive systemic sclerosis (generalized scleroderma). Observation on 120 cases].

Vatti M, Giordano A, Giordano M.
Zeitschrift fur Rheumatologie. ;43(4)171-4.
120 patients with progressive systemic sclerosis (PSS) were studied and subdivided into five groups according to the PSS classification of Giordano et al. ("acute diffuse scleroderma", "intermediate syndrome", "acrosclerosis sensu stricto", "sclerodactylia" and "sclerosis sine scleroderma"). In all
PMID 6495889

Japanese Journal

ネフローゼ症候群を呈し,腎尿細管acidosisを疑わせた全身性硬化症の1剖検例

小林芳夫 [他],村岡松生,東條毅,安倍達,本間光夫,河合俊明,細田泰弘
日本内科学会雑誌 66(2), 186-192, 1977
… PSSの腎病変で,ネフローゼ症候群を呈した症例は少ない.また強皮症状を欠くPSS sine sclerodermaの報告例もまれである.多発性関節炎およびレイノー現象で発症し,強皮症状を示さず, 9年の経過後に,イレウス手術時の生検でPSS sine sclerodermaと診断され,その後ネフローゼ症候群を呈し,尿細管acidosisを疑つた1剖 …
NAID 130000890174

「強皮症を伴わないPSS」

　　[★]

英: PSS sine scleroderma
関: 進行性全身性硬化症

「SINE」

　　[★]

日: 短い散在反復配列、短分散型核内反復配列、短い散在性反復配列
英: short interspersed element, short interspersed nuclear element, short interspersed nucleotide element, SINEs
関: レトロトランスポゾン

quoted from http://en.wikipedia.org/wiki/Long_interspersed_nucleotide_elements#SINEs

Short interspersed repetitive elements or Short interspersed nuclear elements[8] are short DNA sequences (<500 bases) that represent reverse-transcribed RNA molecules originally transcribed by RNA polymerase III into tRNA, rRNA, and other small nuclear RNAs. SINEs do not encode a functional reverse transcriptase protein and rely on other mobile elements for transposition. The most common SINEs in primates are called Alu sequences. Alu elements are 280 base pairs long, do not contain any coding sequences, and can be recognized by the restriction enzyme AluI (hence the name). With about 1,500,000 copies, SINEs make up about 13% of the human genome.[11] While historically viewed as "junk DNA", recent research suggests that in some rare cases both LINEs and SINEs were incorporated into novel genes, so as to evolve new functionality. The distribution of these elements has been implicated in some genetic diseases and cancers.