Literature DB >> 15377950

Sclerosing bone dysplasias: neurologic assessment and management.

Louis M Hofmeyr1, Herman Hamersma.   

Abstract

PURPOSE OF REVIEW: Sclerosing bone dysplasias are rare genetic disorders of bone remodeling in which excessive bone formation takes place, resulting in encroachment on neural structures. The infant usually appears normal at birth, and the first sign of a problem only comes when a neurologic deficit develops, usually in the form of an acute facial palsy. Although less than 300 cases have been published, these conditions should always be considered in the differential diagnosis of facial nerve palsy, especially in children. RECENT
FINDINGS: This review highlights the neurologic presentation and assessment as well as the management of sclerosing bone dysplasias. An exciting development is the recent discovery of the sclerosteosis (SOST) gene, which is involved with excessive bone formation in sclerosteosis and Van Buchem disease. Researchers in bone metabolism and pharmaceutical companies are now utilizing this knowledge to develop a medicine for osteoporosis.
SUMMARY: In children and young adults an acute facial palsy, especially if it is recurrent, as well as a conductive hearing loss may be the first sign of a sclerosing bone dysplasia.

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Year:  2004        PMID: 15377950     DOI: 10.1097/01.moo.0000134441.84110.9e

Source DB:  PubMed          Journal:  Curr Opin Otolaryngol Head Neck Surg        ISSN: 1068-9508            Impact factor:   2.064


  2 in total

1.  Management of trigeminal neuralgia in sclerosteosis.

Authors:  Emerson Magno de Andrade; André Beer-Furlan; Kleber Paiva Duarte; Erich Talamoni Fonoff; Manoel Jacobsen Teixeira
Journal:  Surg Neurol Int       Date:  2013-11-20

2.  Van Buchem disease: First case report in Taiwan.

Authors:  Shang-Fu Hsu; Chen-Chun Lin
Journal:  Medicine (Baltimore)       Date:  2017-12       Impact factor: 1.817

  2 in total

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