Literature DB >> 923406

Hallermann-Streiff syndrome.

P C Donders.   

Abstract

Blodi (1957) and François (1958) recognized this syndrome as a distinct entity differing from the mandibulo-facial dysostosis (Franceschetti's syndrome). Although there are approximately 60 cases reported in the literature, only very few cases have been obtained for histological study. A report of a case with ophthalmopathological examination is given.

Entities:  

Mesh：

Year:  1977        PMID： 923406     DOI： 10.1007/bf00171467

Source DB:  PubMed          Journal:  Doc Ophthalmol        ISSN： 0012-4486            Impact factor:   2.379


  5 in total

1.  [A new syndrome dyscephalia with bird-head and dental abnormalities, nanism, hypotrichosis, cutaneous atrophy, microphthalmia and congenital cataract].

Authors:  J FRANCOIS
Journal:  Boll Ocul       Date:  1958-03

2.  Developmental anomalies of the skull affecting the eye.

Authors:  F C BLODI
Journal:  AMA Arch Ophthalmol       Date:  1957-04

3.  [Dyscephalia with cataracta congenita and hypotrichosis as typical deformity complex].

Authors:  O ULLRICH; H FREMEREY-DOHNA
Journal:  Ophthalmologica       Date:  1953-02       Impact factor: 3.250

4.  [Mandibulofacial dysmorphia with ocular abnormalities].

Authors:  E B STREIFF
Journal:  Ophthalmologica       Date:  1950 Jul-Aug       Impact factor: 3.250

5.  Spontaneous cataract absorption in Hallermann-Streiff syndrome.

Authors:  J R Wolter; D H Jones
Journal:  Ophthalmologica       Date:  1965       Impact factor: 3.250
  5 in total
  2 in total

Review 1.  Genetics of microphthalmos.

Authors:  M Warburg
Journal:  Int Ophthalmol       Date:  1981-08       Impact factor: 2.031

2.  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
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.