Clinical and genetic aspects of a child with monilethrix and visual rehabilitation
Monilethrix is a rare genodermatosis, presented to us with predominant ocular manifestations. The affected proband was typically characterized by severe photophobia, defective vision, and hypotrichosis with brittle and stubby hair. Here, we report a rare case of a 9-year-old male child who has been...
Guardat en:
| Autors principals: | , , , , |
|---|---|
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Wolters Kluwer Medknow Publications
2022-01-01
|
| Col·lecció: | Indian Journal of Ophthalmology. Case Reports |
| Matèries: | |
| Accés en línia: | https://journals.lww.com/10.4103/ijo.IJO_542_21 |
| Etiquetes: |
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|