Literature DB >> 6475869

Syndrome of osteopathia striata, macrocephaly, and cranial sclerosis.

M Robinow, F Unger.   

Abstract

The combination of osteopathia striata, macrocephaly, and cranial sclerosis, variably associated with certain other congenital anomalies, constitutes a rare autosomal dominant malformation syndrome. A new case presented herein demonstrates the natural evolution of the syndrome in infancy and early childhood. Since the macrocephaly is likely to be the initial manifestation, the syndrome should be considered in the differential diagnosis of infants with unexplained macrocephaly.

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Year:  1984        PMID: 6475869     DOI: 10.1001/archpedi.1984.02140470021007

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


  4 in total

1.  Osteopathia striata with cranial sclerosis and hearing loss.

Authors:  K Lüerssen; M Ptok
Journal:  Eur Arch Otorhinolaryngol       Date:  2005-07-12       Impact factor: 2.503

Review 2.  Craniotubular bone disorders.

Authors:  R J Gorlin
Journal:  Pediatr Radiol       Date:  1994

Review 3.  Osteopathia striata with cranial sclerosis.

Authors:  B B Gay; L J Elsas; J B Wyly; M Pasquali
Journal:  Pediatr Radiol       Date:  1994

Review 4.  WTX R353X mutation in a family with osteopathia striata and cranial sclerosis (OS-CS): case report and literature review of the disease clinical, genetic and radiological features.

Authors:  Anna Maria Zicari; Luigi Tarani; Daniela Perotti; Laura Papetti; Francesco Nicita; Natascia Liberati; Alberto Spalice; Guglielmo Salvatori; Federica Guaraldi; Marzia Duse
Journal:  Ital J Pediatr       Date:  2012-06-20       Impact factor: 2.638

  4 in total

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