Literature DB >> 11827425

Lethal prenatal onset infantile cortical hyperostosis (Caffey disease).

J E Dahlstrom1, S M Arbuckle, K Kozlowski, M J Peek, M Thomson, G J Reynolds, D O Sillence.   

Abstract

We describe a sporadic case of lethal prenatal onset infantile cortical hyperostosis (Caffey disease), which resulted in early postnatal death at 30 weeks gestation. The mother presented with antepartum haemorrhage and preterm labour. She was found to have polyhydramnios. The infant showed extensive symmetrical diaphyseal subperiosteal cortical thickening throughout the skeleton with short extremities. Hepatomegaly and lung hypoplasia were present. Currently, in the absence of a specific marker, diagnostic ultrasound offers the only prospect of prenatal diagnosis. This diagnosis should be considered in infants with short angulated long bones, where the diaphyses are irregular and echodense, and where there is no sign of fractures.

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Year:  2001        PMID: 11827425     DOI: 10.1080/00313020120083304

Source DB:  PubMed          Journal:  Pathology        ISSN: 0031-3025            Impact factor:   5.306


  3 in total

1.  A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders.

Authors:  Robert C Gensure; Outi Mäkitie; Catherine Barclay; Catherine Chan; Steven R Depalma; Murat Bastepe; Hilal Abuzahra; Richard Couper; Stefan Mundlos; David Sillence; Leena Ala Kokko; Jonathan G Seidman; William G Cole; Harald Jüppner
Journal:  J Clin Invest       Date:  2005-05       Impact factor: 14.808

2.  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

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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