Results 11 to 20 of about 787 (149)

Lipoid Proteinosis: A Rare Encounter in Dental Office [PDF]

Case Reports in Dentistry, 2015
Lipoid proteinosis is a sporadic congenital metabolic disorder which is characterized by deposition of hyaline material in dermis, submucosal connective tissue, and various internal organs. It has an extremely low prevalence rate with less than 300 cases
Prasannasrinivas Deshpande, Mahima Veeranna Guledgud, Karthikeya Patil, Usha Hegde, Ankita Sahni, Sreeshlya Huchanahalli Sheshanna   +5 more
doaj   +2 more sources

Lipoid proteinosis: A rare entity

Indian Journal of Ophthalmology, 2015
Urbach–Wiethe syndrome or lipoid proteinosis is a rare autosomal recessive disorder characterized histologically by infiltration of Periodic acid Schiff-positive hyaline material in the skin, upper aerodigestive tract, eyelids, and internal organs ...
Bipasha Mukherjee, Pratheeba N Devi
doaj   +2 more sources

Lipoid proteinosis

Indian Journal of Dermatology, 2006
A three and half years old female child with lipoid proteinosis with no history of parental consanguinity and affected siblings has been reported here.
Mukhija Pooja, Singh Shweta, Singh Shailendra, Mukhija R   +3 more
doaj   +5 more sources

Acitretin Treatment for Lipoid Proteinosis [PDF]

Case Reports in Dermatological Medicine, 2012
Lipoid proteinosis (LP) is a rare, autosomal-recessive disease characterized by the hoarseness and widespread cutaneous scarring, more prominent on sun-exposed areas.
Özgür Gündüz, Neriman Şahiner, Pınar Atasoy, Çağrı Şenyücel   +3 more
doaj   +2 more sources

Lipoid proteinosis. [PDF]

BMJ Case Rep, 2017
Singh S, Mittal S, Bhari A, Bhari N.
europepmc   +4 more sources

Association Between Lipoid Proteinosis And Coeliac Disease [PDF]

Dermatology Practical & Conceptual, 2023
Layla Bendaoud, Ihssane Bigjoine, Ouafa Hocar, Said Amal   +3 more
doaj   +2 more sources

A Sporadic Family of Lipoid Proteinosis with Novel ECM1 Gene Mutations

Clinical, Cosmetic and Investigational Dermatology
Yu-Ling Liu, Zeng-Yun-Ou Zhang, Xiao-Mei Chen Department of Dermatology and Venerology, West China Hospital of Sichuan University, Chengdu, People’s Republic of ChinaCorrespondence: Xiao-Mei Chen, Department of Dermatology, West China Hospital of Sichuan
Liu YL, Zhang ZYO, Chen XM
exaly   +2 more sources

Lipoid proteinosis: A review with two case reports

Contemporary Clinical Dentistry, 2015
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, mucous membranes of the upper aerodigestive tract, and internal organs ...
Vishal Kabre, Smitha Rani, Keerthilatha M Pai, Sakshi Kamra   +3 more
doaj   +2 more sources

Lipoid proteinosis (Urbach-Wiethe disease) in two siblings

Indian Dermatology Online Journal, 2014
Lipoid proteinosis is a very rare autosomal recessive disorder characterized by deposition of hyaline material in the skin and the upper aerodigestive tract. Hoarseness of voice occurs very early in life and airway obstruction may occur.
Rekha Thaddanee, Ajeet Kumar Khilnani, Purna Pandya, Mayank Chaturvedi   +3 more
doaj   +2 more sources

Lipoid proteinosis: A rare genodermatosis with multisystemic manifestations-A case report. [PDF]

Clin Case Rep
Waxy facial skin appearance with multiple atrophic ill‐defined, superficial scars of varying size. Key Clinical Message Lipoid proteinosis (LP) is a rare autosomal recessive genodermatosis, which is characterized by the deposition of amorphous hyaline material in various tissues, including the mucosa, visceral organs, and skin. We report a case of a 11‐
Hashmi FN, Huma S, Singireddy H, Zareen N, Suvvari TK, Ansari MH, Sultana N, Hasibuzzaman MA.   +7 more
europepmc   +2 more sources