Lipoid proteinosis in two siblings: A report from India

17Citations
Citations of this article
2Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Lipoid proteinosis is an autosomally recessive genodermatosis characterized by widespread deposition of eosinophilic hyaline-like material in the skin, mucous membranes, and other internal organs. Occurrence of lipoid proteinosis in siblings is very rare. We report two siblings from the Indian subcontinent with the classical features of lipoid proteinosis. Both the siblings had had hoarseness of voice and spontaneous vesicular eruptions healing with atrophic scars since their early childhood. They had diffuse waxy thickening of the skin along with beaded papules along the eyelid margin. The tongue was also infiltrated. Skin biopsy demonstrated periodic acid Schiff (PAS) positive eosinophilic material around the blood vessels and appendages.

Author supplied keywords

Cite

CITATION STYLE

APA

Sethuraman, G., Tejasvi, T., Khaitan, B. K., Handa, K. K., Rao, S., Singh, M. K., … Sharma, V. K. (2003). Lipoid proteinosis in two siblings: A report from India. Journal of Dermatology, 30(7), 562–565. https://doi.org/10.1111/j.1346-8138.2003.tb00434.x

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free