Caffey-Silverman disease

カフィー・シルヴァーマン病

WordNet

1. an impairment of health or a condition of abnormal functioning
2. caused by or altered by or manifesting disease or pathology; "diseased tonsils"; "a morbid growth"; "pathologic tissue"; "pathological bodily processes" (同)morbid, pathologic, pathological

PrepTutorEJDIC

1. (体の)『病気』,疾患 / (精神・道徳などの)病気,病弊
2. 女性の話術芸人 =diseur
3. 病気にかかった / 病的な,不健全な(morbid)

UpToDate Contents

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• 1. 児童虐待の整形外科的症状の鑑別診断differential diagnosis of the orthopedic manifestations of child abuse [show details]
  …mild OI in the acute setting at the time the child presents . Infantile cortical hyperostosis (Caffey disease, Caffey-Silverman disease) is characterized by fever (sometimes as high as 40°C [104ºF]), …
• 2. 小児における不明熱：病因fever of unknown origin in children etiology [show details]
  …persistent viral or parasitic infections in association with prolonged fevers. Infantile cortical hyperostosis (Caffey disease) is an inherited disease characterized by persistent fevers, sometimes as high …
• 3. 小児における血行性骨髄炎：評価および診断hematogenous osteomyelitis in children evaluation and diagnosis [show details]
  …distinguished from osteomyelitis by autonomic dysfunction and normal ESR/CRP. Caffey disease – (infantile cortical hyperostosis) is an inherited disease characterized by fever, subperiosteal bone hyperplasia…
• 4. 小児の不明熱に対するアプローチfever of unknown origin in children evaluation [show details]
  …suggest: Brucellosis Leukemia or lymphoma Osteomyelitis or septic arthritis Infantile cortical hyperostosis Kikuchi-Fujimoto disease It is important to ask, and ask again, specifically about …
• 5. 身体的虐待を受けた疑いのある小児の鑑別診断differential diagnosis of suspected child physical abuse [show details]
  …absent: Normal bone variants ; Periosteal reaction from drugs, infection, or infantile cortical hyperostosis (Caffey disease) The differential diagnosis of burns in possible victims of child abuse includes…

English Journal

• Birth Order and Maternal Age for Reported Cases of Severe Prenatal Cortical Hyperostosis (Caffey–Silverman Disease)

• Engel RR, Cifuentes RF.
• AJP reports. 2017 07;7(3)e174-e180.
• The spectrum of prenatal cortical hyperostosis includes a mild phenotype that typically presents after 35 weeks of gestation, and a severe form that presents earlier. The skeletal and systemic manifestations of the severe phenotype remain unexplained. A review of reported cases indicates that older
• PMID 29142783

• Hyperostosis in siblings.

• Spranger JW, Lausch E.
• South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde. 2016 May;106(6 Suppl 1)S98-9.
• Infantile cortical hyperostosis - Caffey-Silverman disease - is a familial disorder manifesting in the late fetal period or infancy with excessive periosteal bone formation. Signs and symptoms regress spontaneously within months and result in expanded, deformed bones. The paucity of clinical symptom
• PMID 27245539

• [Infantile cortical hyperostosis: Case report].

• Rodríguez M, Martínez LE, Cortés J, de Uña A, Vega V, Acosta M.
• Revista chilena de pediatria.  ;87(5)401-405.
• Infantile Cortical Hyperostosis, or Caffey-Silverman disease, is a rare condition characterised by generalised bone proliferation mediated by an acute inflammatory process. Diagnosis can be made through clinical evaluation and X-ray studies. The course is generally self-limiting and prognosis is exc
• PMID 27020539

Related Links

• Caffey disease - Genetics Home Reference - NIH

Caffey disease has been estimated to occur in approximately 3 per 1,000 infants worldwide. A few hundred cases have been described in the medical literature. Researchers believe this condition is probably underdiagnosed because it

• Caffey Disease or Infantile Cortical Hyperostosis: A Case Report

Caffey disease, also known as Infantile Cortical Hyperostosis is a self-limiting disorder. It is characterized by a triad of systemic symptoms (irritability and fever), soft tissue swelling and underlying cortical bone thickening.

• OMIM Entry - # 114000 - CAFFEY DISEASE

In affected individuals and obligate carriers from 3 unrelated families with Caffey disease, Gensure et al. (2005) identified heterozygosity for an arg836-to-cys mutation in the COL1A1 gene (R836C; 120150.0063), involving the triple-helical domain of the alpha-1 chain of type I collagen. ...

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★リンクテーブル★

リンク元	「カフィー・シルヴァーマン病」
関連記事	「disease」

「カフィー・シルヴァーマン病」

　　[★]

英

Caffey-Silverman disease

関

カフィー症候群

「disease」

　　[★]

• n.

疾患：illnessより厳密な概念。「ある臓器に明確な障害が確認され、それによって症状が出ているとはっきり説明できる場合」 (PSY.9)

特定の原因、病態生理、症状、経過、予後、病理組織所見が全てそろった場合 (PSY.9)

• something that is very wrong with people's attitudes, way of life or with society.

関

ail、ailment、disease entity、disorder、ill、illness、malady、sick、sickness

• 注意

disease ≠ illness ≠ disorder