Literature DB >> 15347328

Hallermann-Streiff syndrome: a case review.

A Mirshekari1, F Safar.   

Abstract

Hallermann-Streiff Syndrome is a rare genetic disorder that is characterized primarily by head and face abnormalities. Patients show bird-like facies, dental abnormalities, and hypotrichosis with various ophthalmic abnormalities. We report here a 26-year-old woman with Hallermann-Streiff Syndrome and review the literature.

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Year:  2004        PMID： 15347328     DOI： 10.1111/j.1365-2230.2004.01572.x

Source DB:  PubMed          Journal:  Clin Exp Dermatol        ISSN： 0307-6938            Impact factor:   3.470


  3 in total

1.  Surgical correction of Hallermann-Streiff syndrome: a case report of esotropia, entropion, and blepharoptosis.

Authors:  Won-Kyung Cho; Joo Wan Park; Mi Ra Park
Journal:  Korean J Ophthalmol       Date:  2011-03-14

2.  Hallermann-Streiff syndrome with severe bilateral enophthalmos and radiological evidence of silent brain syndrome: a new congenital silent brain syndrome?

Authors:  Paolo Nucci; Carlo de Conciliis; Matteo Sacchi; Massimiliano Serafino
Journal:  Clin Ophthalmol       Date:  2011-07-04

3.  Hallermann-Streiff syndrome with uncommon ocular features, ultrasound biomicroscopy and optical coherence tomography findings: A case report.

Authors:  Wei Shen; Min Dai; Yunshan Su; Qing Zhang; Hongsong Li
Journal:  Medicine (Baltimore)       Date:  2019-12       Impact factor: 1.889
  3 in total

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