Touraine–Solente–Gole syndrome: Clinical manifestation with bilateral true eyelid ptosis

Touraine–Solente–Gole syndrome (pachydermoperiostosis [PDP] or primary idiopathic hypertrophic osteoarthropathy [HOA]) is a rare hereditary disorder that is characterized by a triad of manifestations that consists of skin changes (pachydermia), abnormal bone and joint manifestations (periostosis and...

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Detalles Bibliográficos
Autores principales: Akaranuchat, Nutthawut, Limsuvan, Papassorn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Case Reports and Short Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7061552/
https://www.ncbi.nlm.nih.gov/pubmed/32158879
http://dx.doi.org/10.1016/j.jpra.2019.04.004

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7061552/
https://www.ncbi.nlm.nih.gov/pubmed/32158879
http://dx.doi.org/10.1016/j.jpra.2019.04.004

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