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...

Celý popis

Podrobná bibliografie

Hlavní autoři:	Monisha Mohan, Shashikant Shetty, Vijayalakshmi Perumalsamy, C Prakash, Periasamy Sundaresan
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Wolters Kluwer Medknow Publications 2022-01-01
Edice:	Indian Journal of Ophthalmology. Case Reports
Témata:	cataract corneal pannus hypotrichosis monilethrix regularly bended ribbon sign
On-line přístup:	https://journals.lww.com/10.4103/ijo.IJO_542_21
Tagy:	Přidat tag Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!