Lipoid proteinosis: Ultrastructural and biochemical studies
References (24)
- et al.
Hyalinosis cutis et mucosae: a histochemical staining and analytical biochemical study
J Invest Dermatol
(1969) - et al.
Ultrastructure and composition of connective tissue in hyalinosis cutis et mucosae skin
J Invest Dermatol
(1984) - et al.
Lipoid proteinosis: in vivo and in vitro evidence for a lysosomal storage disease
J Invest Dermatol
(1981) - et al.
Collagen biosynthesis by human skin fibroblasts. I. Optimization of the culture conditions for synthesis of type I and type III procollagens
Biochem Biophys Acta
(1980) - et al.
Modified procedure for the assay of 3H- or 14C-labeled hydroxyproline
Anal Biochem
(1966) A rapid and sensitive method for quantitation of microgram quantities of protein utilizing the principle of protein-binding dye
Anal Biochem
(1976)- et al.
Isolation of cDNA and genomic clones encoding human pro-alphal(III) collagen: partial charac terization of the 3' end region of the gene
J Biol Chem
(1985) Urbach-Wiethe disease (lipoglycoproteinosis; lipoid proteinosis; hyalinosis cutis et mucosae): a review
Acta Derm Venereol (Stockh)
(1973)Visceral involvement in lipoid proteinosis
Arch Dermatol
(1967)- et al.
Lipoidosis cutis et mucosae
Virchows Arch [Pathol Anat]
(1929)
Lipoid proteinosis
Int J Dermatol
(1978)
Oropharyngeal and laryngeal lesion in lipoid proteinosis
J Laryngol Otol
(1983)
Cited by (60)
Ultrastructural aspects of the skin in lipoid proteinosis (Urbach-Wiethe disease)
2021, Anais Brasileiros de DermatologiaCutaneous deposits
2009, Weedon's Skin Pathology: Third EditionUrbach-Wiethe disease
2009, Medicina ClinicaThree-dimensional imaging reveals major changes in skin microvasculature in lipoid proteinosis and lichen sclerosus
2005, Journal of Dermatological ScienceEyelid tumour and juvenile hyaline fibromatosis
2005, British Journal of Plastic SurgeryCitation Excerpt :Radiologically generalised osteoporosis and progressive resorption of the carpal bones is observed.23 Lipoid proteinosis should also be excluded and is characterised by amorphous matrix accumulation, which is acellular.4,24 The more aggressive form (ISH) must be differentiated from infantile myofibromatosis (IMF),3,4,16 also known as congenital generalised fibromatosis (CGF).
Supported in part by U.S. Public Health Service, National Institutes of Health, Grants AR-28450, GM-28833, and AR-35297, and by a grant from the American Society of Dermatologic Surgery, awarded by the Dermatology Foundation.
Copyright © 1987 Published by Mosby, Inc.