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复发性卡菲皮质增生症与持续性畸形

Recurrent Caffey's cortical hyperostosis and persistent deformity.

作者信息

Blank E

出版信息

Pediatrics. 1975 Jun;55(6):856-60.

PMID:1094401
Abstract

A boy, age 12 years, who had infantile cortical hyperostosis has continued to have occasional aches and new cortical thickenings in his arms and legs. His mandible is undergrown and his ribs have an abnormal slope. Recurrence of Caffey's cortical hyperostosis and persistent deformity have been observed in other children and young adults. Some unexplained cases of late cortical thickening and pain may be due to Caffey's disease.

摘要

一名12岁曾患婴儿骨皮质增生症的男孩,手臂和腿部仍偶尔疼痛并有新的骨皮质增厚。他的下颌发育不全,肋骨有异常倾斜。在其他儿童和年轻人中观察到了卡菲骨皮质增生症的复发和持续性畸形。一些不明原因的晚期骨皮质增厚和疼痛病例可能归因于卡菲病。

相似文献

1
Recurrent Caffey's cortical hyperostosis and persistent deformity.复发性卡菲皮质增生症与持续性畸形
Pediatrics. 1975 Jun;55(6):856-60.
2
Sporadic congenital infantile cortical hyperostosis (Caffey's disease).散发性先天性婴儿皮质增生症(卡菲氏病)。
Am J Perinatol. 1998;15(11):629-33. doi: 10.1055/s-2007-994081.
3
Infantile cortical hyperostosis of the ribs (Caffey's disease) without mandibular involvement.无下颌骨受累的婴儿肋骨皮质增生症(卡菲病)
Pediatr Radiol. 1983;13(4):236-8. doi: 10.1007/BF00973165.
4
Infantile cortical hyperostosis (Caffey's disease).婴儿骨皮质增生症(卡菲氏病)。
Afr J Med Med Sci. 1978 Mar;7(1):37-41.
5
Vesico-ureteric reflux in Caffey's disease (Infantile cortical hyperostoses).
Ann Radiol (Paris). 1967;10(9):687-8.
6
[Familial infantile cortical hyperostosis (Caffey's disease) with osteolytic lesions of the skull].
Arch Fr Pediatr. 1992 Jun-Jul;49(6):525-8.
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Familial Caffey's disease and late recurrence in a child.
Clin Genet. 1991 Oct;40(4):329-35. doi: 10.1111/j.1399-0004.1991.tb03104.x.
8
Prenatal infantile cortical hyperostosis (Caffey's disease): a 'hepatic myeloid hyperplasia-pulmonary hypoplasia sequence' can explain the lethality of early onset cases.产前婴儿皮质增生症(卡菲氏病):“肝髓样增生-肺发育不全序列”可解释早发型病例的致死性。
Prenat Diagn. 2005 Oct;25(10):939-44. doi: 10.1002/pd.1235.
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Caffey's disease in an infant.一名婴儿患婴儿骨皮质增生症。
J Coll Physicians Surg Pak. 2011 Oct;21(10):634-6. doi: 10.2011/JCPSP.634636.
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[Prenatal diagnosis of Caffey's disease (infantile cortical hyperostosis)].[婴儿骨皮质增生症(卡菲氏病)的产前诊断]
Klin Padiatr. 1985 Nov-Dec;197(6):473-6. doi: 10.1055/s-2008-1034024.

引用本文的文献

1
Radiographic overlap of recurrent Caffey disease and chronic recurrent multifocal osteomyelitis (CRMO) with considerations of molecular origins.复发型卡斐氏病与慢性复发性多灶性骨髓炎的影像学重叠,并考虑其分子起源。
Pediatr Radiol. 2020 May;50(5):618-627. doi: 10.1007/s00247-019-04590-3. Epub 2019 Dec 23.
2
Infantile cortical hyperostosis and COL1A1 mutation in four generations.四代同堂的婴儿性皮质增生症和 COL1A1 基因突变。
Eur J Pediatr. 2011 Nov;170(11):1385-90. doi: 10.1007/s00431-011-1463-0. Epub 2011 May 13.
3
Scintigraphic and radiological correlative and confirmative features obviating invasive biopsy in Caffey's disease.
骨皮质增生症中避免进行侵入性活检的闪烁扫描和放射学相关及确诊特征。
Indian J Nucl Med. 2010 Jan;25(1):20-2. doi: 10.4103/0972-3919.63595.
4
A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders.婴儿皮质增生症(卡菲病)中的一种新型COL1A1突变扩大了胶原相关疾病的范围。
J Clin Invest. 2005 May;115(5):1250-7. doi: 10.1172/JCI22760.
5
MRI findings in Caffey's disease.婴儿骨皮质增生症的磁共振成像表现。
Pediatr Radiol. 1994;24(5):325-7. doi: 10.1007/BF02012117.
6
Familial infantile cortical hyperostosis in a large Canadian family.一个加拿大大家庭中的家族性婴儿皮质增生症
Can Med Assoc J. 1984 May 1;130(9):1172-4.
7
Infantile cortical hyperostosis.婴儿骨皮质增生症
Arch Dis Child. 1976 Aug;51(8):589-95. doi: 10.1136/adc.51.8.589.
8
Infantile cortical hyperostosis with raised immunoglobulins.伴有免疫球蛋白升高的婴儿皮质增生症。
Arch Dis Child. 1978 May;53(5):426-8. doi: 10.1136/adc.53.5.426.