HYPERKERATOSIS LENTICULARIS PERSTANS PDFAugust 10, 2020
A collection of disease information resources and questions answered by our Genetic and Rare Diseases Information Specialists for Hyperkeratosis lenticularis . Flegel disease is also known as ‘hyperkeratosis lenticularis perstans’. It was first described by Flegel in It is characterised by red-brown papules with. Hyperkeratosis lenticularis perstans (HLP) is a rare cutaneous disorder occurring in older persons and manifested by multiple benign pink to reddish-brown.
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None, Conflict of Interest: Case report of a rare entity.
How to cite this article: Indian J Dermatol ; How to cite this URL: Discrete, follicular papular lesions on dorsa of feet Click here to view. Similar lesions on forearms Click here to view.
Lesions on thighs Click here to view. Few lesions of similar morphology on trunk Click here to view. Mild improvement with treatment noted after 3 weeks Click here to view. Frenk E, Tapernoux B.
Flegel disease pathology | DermNet NZ
Hyperkeratosis lenticularis perstans Flegel. An autosomal dominant skin disease due to lack of a keratinocyte organelle. The genetics of hyperkeratosis lenticularis perstans. Long-standing spiny papules on the lower extremities.
Flegel disease, or hyperkeratosis lenticularis perstans HLP. Multiple asymptomatic hyperkeratotic papules on the lower part of the legs.
Hyperkeratosis lenticularis perstans: Case report of a rare entity Patel KB – Indian J Dermatol
Hyperkeratosis lenticularis perstans HLP Flegel disease. An unusual generalized form of hyperkeratosis lenticularis perstans Flegel’s disease. Wien Klin Wochenschr ; Unilateral hyperkeratosis lenticularis perstans Flegel’s disease. J Am Acad Dermatol ; Degenerative diseases and perforating disorders. Lever’s Histopathology of the skin, 10th ed.
Wolters Kluwer India; Search Pubmed for Patel KB.