Objectives Lipoid proteinosis (LP) is a rare autosomal recessive disorder characterized by
deposits of hyaline material within skin and mucous membranes of the upper aerodigestive …

Lipoid proteinosis, a very rare autosomal recessive genodermatosis, results in hyaline
material deposition in the skin and mucous membrane of various organs leading to …

Objectives Lipoid proteinosis (LP) is a rare autosomal recessive genodermatosis
characterized by mucocutaneous lesions and hoarseness that develop in early childhood …

Lipoid proteinosis (LP) is a rare autosomal recessive genodermatosis associated with
deposition of periodic acid-Shiff (PAS)-positive hyaline material in skin, mucosa, and other …

Lipoid proteinosis (LP) is a rare autosomal recessive genodermatoses characterized by
deposition of amorphous hyaline material in different parts of the body, especially the skin …

Lipoid proteinosis (hyalinosis cutis et mucosae) is a rare, autosomal recessive disease. The
main clinicopathological features comprise skin and mucous membrane infiltration and …

Lipoid proteinosis (LP) is a rare autosomal recessive genodermatosis characterized by
deposition of amorphous hyaline material in different parts of the body, especially the skin …

Lipoid proteinosis (LP) is a rare autosomal-recessive genodermatosis, characterized by the
deposition of amorphous hyaline-like material in different parts of the body, especially the …

This report describes the diagnostic process of a rare disorder in a Brazilian female child.
The patient presented initially as a 7-year-old with multiple whitish submucosal nodules of a …

Objectives Lipoid proteinosis (LP) is a rare autosomal recessive disorder characterized by
the accumulation of hyaline‐like material in the skin, oral mucosa, larynx, and brain. This …