Literature DB >> 10064204

Sporadic congenital infantile cortical hyperostosis (Caffey's disease).

K I Al-Tawil1, G S Ahmed, M M Al-Hathal, M A Al-Zuwayed.   

Abstract

Prognosis of congenital infantile cortical hyperostosis (Caffey's disease) is poor particularly in premature babies. Two cases are presented of congenital Caffey's disease in premature babies. The first baby was hydropic at birth and had cortical hyperostosis involving the mandible and long bones of right upper limb and both lower limbs. The second baby had cortical hyperostosis of the nasal bones causing severe nasal nonchoanal stenosis that needed surgery, in addition to involvement of long bones of the four extremities. Both babies recovered from the disease and were discharged home well. These cases suggest that the improved outcome of congenital of infantile cortical hyperostosis may reflect improvement of neonatal mechanical ventilation and availability of neonatal total parenteral nutrition.

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Year:  1998        PMID: 10064204     DOI: 10.1055/s-2007-994081

Source DB:  PubMed          Journal:  Am J Perinatol        ISSN: 0735-1631            Impact factor:   1.862


  3 in total

1.  Caffey's disease: an unusual cause for concern.

Authors:  F J Shannon; M Murphy; I Atchia; E Phelan; E E Fogarty
Journal:  Ir J Med Sci       Date:  2007-05-03       Impact factor: 1.568

2.  Scintigraphic and radiological correlative and confirmative features obviating invasive biopsy in Caffey's disease.

Authors:  M Ranadheer; Santhi Bhushan Murari; N Sujith; Pushpalatha Sudhakar; Vvs Prabhakar Rao
Journal:  Indian J Nucl Med       Date:  2010-01

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

Authors:  Rolf R Engel; Raul F Cifuentes
Journal:  AJP Rep       Date:  2017-09-11
  3 in total

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