Literature DB >> 998829

Frontometaphyseal dysplasia: evidence for autosomal dominant inheritance.

E G Kassner, J O Haller, V H Reddy, A Mitarotundo, I Katz.   

Abstract

Frontometaphyseal dysplasia is a syndrome that encompasses cranial hyperostosis, abnormal tubulation of cylindrical bones, and other skeletal and extraskeletal abnormalities. The most striking features are overgrowth of the supraorbital ridges which results in a Mephistophelian facial appearance and a radiographic configuration of the skull that has been likened to a soldier's helmet. Most patients have severe hearing loss, defective dentition, poorly developed musculature, and joint contractures. Dominant inheritance has been suggested in previous reports, but an appropriate pedigree has been documented in only one family. This paper describes three additional patients in two unrelated families: (1) an 8-year-old boy whose mother has mild metaphyseal dysplasia and several minor skeletal abnormalities that have occurred in patients with the syndrome; and (2) two maternal half-brothers. These cases provide additional evidence that frontometaphyseal dysplasia is an autosomal dominant trait with variable penetrance.

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Year:  1976        PMID: 998829     DOI: 10.2214/ajr.127.6.927

Source DB:  PubMed          Journal:  AJR Am J Roentgenol        ISSN: 0361-803X            Impact factor:   3.959


  3 in total

Review 1.  Craniotubular bone disorders.

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

2.  Frontometaphyseal dysplasia: autosomal dominant or X-linked?

Authors:  P Beighton; H Hamersma
Journal:  J Med Genet       Date:  1980-02       Impact factor: 6.318

3.  Treatment of obstructive uropathy in one of three young brothers suffering from Gorlin-Cohen syndrome: a case report.

Authors:  Ioannis Vakalopoulos; Spyridon Kampantais; Panagiotis Dimopoulos; Christos Papastavros; Vasileios Katsikas
Journal:  BMC Urol       Date:  2012-01-10       Impact factor: 2.264

  3 in total

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