Literature DB >> 15530943

Dysmorphology and the orbital region: a practical clinical approach.

Hélène Dollfus1, Alain Verloes.   

Abstract

Dysmorphology is the field of medicine focusing on congenital developmental abnormalities due to exogenous teratogens, chromosomal anomalies, or to a defect in a single gene. Numerous syndromes have been reported and a growing number of genes or chromosomal anomalies are identified. The clinical observation of the face remains an essential part of the clinical evaluation of the patients. The orbital region, as other regions of the face, should be systematically evaluated. Orbital malformations can be isolated or part of a syndrome. In the diagnostic process, the orbital anomaly can be classified as a major feature (essential for the diagnosis), a moderate feature (important but not essential for the diagnosis), or a minor feature (contributing weakly to the diagnosis). The diagnoses of the main orbital anomalies in dysmorphology are reviewed and illustrated with relevant examples of syndromes that are presented as well as the usual landmarks used in clinical practice. Abnormal position of the eyes in syndromes such as hypertelorism, hypotelorism, primary or secondary telecanthus, asymmetry, and proptosis are discussed. Eyelid anomalies, such as cryptophthalmos, ablepharon, blepharophimosis, euryblepharon, or anomalies at the level of the eyelashes and eyebrows are described.

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Year:  2004        PMID: 15530943     DOI: 10.1016/j.survophthal.2004.08.001

Source DB:  PubMed          Journal:  Surv Ophthalmol        ISSN: 0039-6257            Impact factor:   6.048


  6 in total

1.  A useful flap combination in wide and complex defect reconstruction of the medial canthal region: Glabellar rotation and nasolabial V-Y advancement flaps.

Authors:  Erol Kesiktas; Cengiz Eser; Eyüphan Gencel; Emrah Efe Aslaner
Journal:  Plast Surg (Oakv)       Date:  2015       Impact factor: 0.947

2.  Clinical and Molecular Update on the Fourth Reported Family with Hamamy Syndrome.

Authors:  André Mégarbané; Sayeeda Hana; Hala Mégarbané; Christel Castro; Sylvain Baulande; Audrey Criqui; Nathalie Roëckel-Trevisiol; Christel Dagher; Mahmoud Taleb Al-Ali; Jean-Pierre Desvignes; Daniel Mahfoud; Stephany El-Hayek; Valérie Delague
Journal:  Mol Syndromol       Date:  2021-08-31

3.  MRI study of minor physical anomaly in childhood autism implicates aberrant neurodevelopment in infancy.

Authors:  Charlton Cheung; Grainne M McAlonan; Yee Y Fung; Germaine Fung; Kevin K Yu; Kin-Shing Tai; Pak C Sham; Siew E Chua
Journal:  PLoS One       Date:  2011-06-08       Impact factor: 3.240

4.  Genetic architecture of orbital telorism.

Authors:  Maria J Knol; Mikolaj A Pawlak; Sander Lamballais; Natalie Terzikhan; Edith Hofer; Ziyi Xiong; Caroline C W Klaver; Lukas Pirpamer; Meike W Vernooij; M Arfan Ikram; Reinhold Schmidt; Manfred Kayser; Tavia E Evans; Hieab H H Adams
Journal:  Hum Mol Genet       Date:  2022-05-04       Impact factor: 5.121

5.  Congenital fusion of jaw and ankyloblepharon filiforme adnatum: malformation and multiple systems anomaly.

Authors:  Mallika P Reddy; S R Raghu
Journal:  Indian J Plast Surg       Date:  2012-09

6.  Basal encephalocele in an adult patient presenting with minor anomalies: a case report.

Authors:  Naoyuki Harada; Masaaki Nemoto; Chikao Miyazaki; Kosuke Kondo; Hiroyuki Masuda; Jun Nomoto; Nobuo Sugo; Takao Kuroki
Journal:  J Med Case Rep       Date:  2014-01-27
  6 in total

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