Literature DB >> 19218897

Hallermann-Streiff Syndrome: a case report from Turkey.

Zuhal Kirzioğlu1, Derya Ceyhan.   

Abstract

Hallermann-Streiff Syndrome (HSS) is a rare disorder characterized primarily by head and face abnormalities, with dental abnormalities also present in 50-80 percent of cases. The first description seems to have been made by Aubry in 1893. HSS was first described completely in 1948 by Hallermann, and then in 1950 by Streiff. We report a 4-year-old girl with HSS, presenting oro-dental characteristics and describe the treatment modalities. An interdisciplinary approach including early preventive-care programmes, detailed oral hygiene instructions, dietary recommendations, counselling of the parents and regular dental visits are the essential procedures.

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Mesh:

Year:  2009        PMID: 19218897

Source DB:  PubMed          Journal:  Med Oral Patol Oral Cir Bucal        ISSN: 1698-4447


  2 in total

1.  A familial study of Hallermann-Streiff-François syndrome.

Authors:  E Epée; D Beleho; A T Bitang; V A Njami; C Bengondo; Côme Ebana Mvogo
Journal:  Int Med Case Rep J       Date:  2017-06-10

2.  Oculodentodigital dysplasia.

Authors:  Dharmil C Doshi; Purvi K Limdi; Nilesh V Parekh; Neepa R Gohil
Journal:  Indian J Ophthalmol       Date:  2016-03       Impact factor: 1.848

  2 in total

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