Literature DB >> 3044797

Infantile cortical hyperostosis associated with the Wiskott-Aldrich syndrome.

M Abinun1, M Mikuska, B Filipović.   

Abstract

A case report of an infant with the Wiskott-Aldrich syndrome and clinical and radiological features of infantile cortical hyperostosis (Caffey disease) is presented. This is the third case described of the association of these two rare disorders and gives further support to the role of an immunologic defect in the pathogenesis of infantile cortical hyperostosis.

Entities:  

Mesh：

Year:  1988        PMID： 3044797     DOI： 10.1007/BF00441979

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN： 0340-6199            Impact factor:   3.183


  8 in total

1.  Aldrich's syndrome. Report of a case with subperiosteal hemorrhage.

Authors:  A M RIVERA; F C BIEHUSEN
Journal:  J Pediatr       Date:  1960-07       Impact factor: 4.406

2.  Pedigree demonstrating a sex-linked recessive condition characterized by draining ears, eczematoid dermatitis and bloody diarrhea.

Authors:  R A ALDRICH; A G STEINBERG; D C CAMPBELL
Journal:  Pediatrics       Date:  1954-02       Impact factor: 7.124

3.  Raised immunoglobulin levels and thrombocytosis in infantile cortical hyperostosis.

Authors:  I J Temperley; S J Douglas; J P Rees
Journal:  Arch Dis Child       Date:  1972-12       Impact factor: 3.791

4.  Infantile cortical hyperostosis associated with thrombocythaemia.

Authors:  D Pickering; B Cuddigan
Journal:  Lancet       Date:  1969-08-30       Impact factor: 79.321

5.  Vitamin E deficiency and thrombocytosis in Caffey's disease.

Authors:  B R Keeton
Journal:  Arch Dis Child       Date:  1976-05       Impact factor: 3.791

6.  Wiskott-Aldrich syndrome associated with idiopathic infantile cortical hyperostosis (Caffey's disease).

Authors:  G McEnery; F W Nash
Journal:  Arch Dis Child       Date:  1973-10       Impact factor: 3.791

7.  Infantile cortical hyperostosis with raised immunoglobulins.

Authors:  V Ramchander; R Ramkissoon
Journal:  Arch Dis Child       Date:  1978-05       Impact factor: 3.791

8.  Caffey's disease revisited. Further evidence for autosomal dominant inheritance with incomplete penetrance.

Authors:  R A Saul; W H Lee; R E Stevenson
Journal:  Am J Dis Child       Date:  1982-01
  8 in total
  2 in total

Review 1.  The Wiskott-Aldrich syndrome.

Authors:  H D Ochs
Journal:  Clin Rev Allergy Immunol       Date:  2001-02       Impact factor: 8.667

2.  Severe combined immunodeficiency in Serbia and Montenegro between years 1986 and 2010: a single-center experience.

Authors:  Srdjan Pasic; Dragana Vujic; Dobrila Veljković; Bojana Slavkovic; Marija Mostarica-Stojkovic; Predrag Minic; Aleksandra Minic; Goran Ristic; Silvia Giliani; Anna Villa; Cristina Sobacchi; Desa Lilić; Mario Abinun
Journal:  J Clin Immunol       Date:  2014-02-01       Impact factor: 8.317
  2 in total

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