Advanced search
Publication Cover
Journal of Obstetrics and Gynaecology Volume 29, 2009 - Issue 1
Submit an article Journal homepage
49
Views
0
CrossRef citations to date
0
Altmetric
Obstetric Case Reports

Prenatal cortical hyperostosis (Caffey disease) with Down syndrome

N. D. Kroon Department of Obstetrics and Gynaecology, Wexham Park Hospital, Slough, Berkshire, SL2 4HL, UKCorrespondence[email protected]
,
F. Smith Department of Neonatalogy, Wexham Park Hospital, Slough, Berkshire, SL2 4HL, UK
,
R. Sanghavi Department of Neonatalogy, Wexham Park Hospital, Slough, Berkshire, SL2 4HL, UK
&
P. Sarkar Department of Obstetrics and Gynaecology, Wexham Park Hospital, Slough, Berkshire, SL2 4HL, UK
Pages 57-58 | Published online: 02 Jul 2009

References

  • Bercau G, Gonzalez M, Afriat R, et al. The difficulty of diagnosing Caffey's disease in utero. Apropos of a case simulating lethal osteogenesis imperfecta. Annales de pédiatrie (Paris) 1991; 38: 15–18
  • Dahlstrom J E, Arbuckle S M, Kozlowski K, et al. Lethal prenatal onset infantile cortical hyperostosis (Caffey disease). Pathology 2001; 33: 521–525
  • Drinkwater B M, Crino J P, Garcia J, et al. Recurrent severe infantile cortical hyperostosis (Caffey disease) in siblings. Prenatal Diagnosis 1997; 17: 773–776
  • Gensure R C, Makitie O, Barclay C, et al. A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders. The Journal of clinical investigation 2005; 115: 1250–1257
  • Herman T E. Antenatal-onset infantile cortical hyperostosis and nonimmune hydrops. Journal of perinatology: Official Journal of the California Perinatal Association 1996; 16(2 Part 1)137–139
  • Lecolier B, Bercau G, Gonzales M, et al. Radiographic, haematological, and biochemical findings in a fetus with Caffey disease. Prenatal Diagnosis 1992; 12: 637–641
  • Maclachlan A K, Gerrard J W, Houston C S, et al. Familial infantile cortical hyperostosis in a large Canadian family. Canadian Medical Association journal 1984; 130: 1172–1174
  • Pickering D, Cuddigan B. Infantile cortical hyperostosis associated with thrombocythaemia. Lancet 1969; 2: 464–465
  • Saul R A, Lee W H, Stevenson R E. Caffey's disease revisited. Further evidence for autosomal dominant inheritance with incomplete penetrance. American Journal of Diseases of Children 1982; 136: 55–60
  • Schweiger S, Chaoui R, Tennstedt C, et al. Antenatal onset of cortical hyperostosis (Caffey disease): case report and review. American Journal of Medical Genetics: Part A 2003; 120: 547–552
  • Wright J R, Jr, Van den Hof M C, Macken M B. Prenatal infantile cortical hyperostosis (Caffey's disease): a ‘hepatic myeloid hyperplasia-pulmonary hypoplasia sequence’ can explain the lethality of early onset cases. Prenatal Diagnosis 2005; 25: 939–944

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.