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

RATIONALE: Hallermann-Streiff syndrome (HSS) is a rare congenital disorder characterized by craniofacial malformations, sparse hair, degenerative skin changes, eye abnormalities, dental defects, and proportionate short stature. PATIENT CONCERNS: A 24-year-old Chinese male patient presented to the op...

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Detalles Bibliográficos
Autores principales: Shen, Wei, Dai, Min, Su, Yunshan, Zhang, Qing, Li, Hongsong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
7300
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6919421/
https://www.ncbi.nlm.nih.gov/pubmed/31804366
http://dx.doi.org/10.1097/MD.0000000000018272

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6919421/
https://www.ncbi.nlm.nih.gov/pubmed/31804366
http://dx.doi.org/10.1097/MD.0000000000018272

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