Hallermann-Streiff syndrome (HSS) is a rare congenital abnormality affecting mostly the head and face area. Craniofacial deformities, which are present in 98-99% of cases, are the principal abnormalities detected. We focus here on a particular subset of these deformities: atrophy of the skin of the centre of the face and nose. Two patients diagnosed with HSS were treated in our department. Both patients underwent nasal lipofilling to treat the atrophy of the nasal skin, as described by Nguyen et al. In both cases, a satisfactory improvement in nasal skin colour and texture was observed. A functional gain was also reported by the parents and observed during follow-up consultations. Lipofilling thus appears to be an excellent option for treating craniofacial deformities in children.
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http://dx.doi.org/10.1016/j.ijom.2015.06.020 | DOI Listing |
Front Pediatr
December 2024
Soins Intensifs Pédiatriques, Département Femme-Mère-Enfant, Centre Hospitalier Universitaire Vaudois et Université de Lausanne, Lausanne, Suisse.
[This corrects the article DOI: 10.3389/fped.2022.
View Article and Find Full Text PDFTwin Res Hum Genet
November 2023
Department of Psychology, California State University, Fullerton, California, USA.
The circumstances and subsequent life events of the first twins to have been born in different countries are examined. Given that both twins were born in the United Kingdom, their common citizenship was never questioned. In contrast, twins born in Canada to a legally married gay transnational couple - composed of one American and one Israeli - were assigned as citizens of different nations and their parents were regarded as if unmarried.
View Article and Find Full Text PDFActa Neurol Belg
February 2024
Translational Genomics Laboratory, Department of Biosciences, COMSATS University Islamabad, Islamabad, Pakistan.
Cornea
July 2023
Department of Ophthalmology, University of Washington, Seattle, WA.
Purpose: We describe the management of Hallermann-Streiff syndrome in monozygotic female twins with congenital cataracts, exudative retinal detachments, and 1 case of corneal descemetocele with associated dellen and subsequent perforation.
Methods: This study was a case report and review of the literature.
Results: Twins 1 and 2 exhibited all 7 cardinal characteristics of Hallermann-Streiff syndrome, presenting with spontaneous lenticular resorption, anterior uveitis, and glaucoma.
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