G Akoglu, A Karaduman, S Ergin… - Journal of …, 2011 - informahealthcare.com 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 tissues. LP is caused by loss-of-function mutations in the extracellular matrix protein 1 gene (ECM1). ... Cited by 1 - Related articles - All 3 versions
[HTML] from diagnosticpathology.orgM Nasir, A Latif, M Ajmal, R Qamar… - Diagnostic …, 2011 - diagnosticpathology.org Lipoid proteinosis is a rare autosomal recessive disease characterized by cutaneous and mucosal lesions and hoarseness appearing in early childhood that is caused by homozygous or compound heterozygous mutations in the ECM1 gene located on chromosome 1q21. The aim of the ... Cached
[HTML] from jisppd.comS Mainali, R Nayak… - Journal of Indian Society of Pedodontics …, 2011 - Medknow Lipoid proteinosis, a very rare autosomal recessive genodermatosis, results in hyaline material deposition in the skin and mucous membrane of various organs leading to multisystem involvement. A case report of a 12-year-old female child is presented here who showed ... Related articles - All 3 versions
[PDF] from biomedcentral.comM Salih, K Abu-Amero, S Alrasheed… - BMC Medical …, 2011 - biomedcentral.com Mustafa A. Salih (mustafsalih@ksu.edu.sa) Khaled K. Abu-Amero (abuamero@gmail.com) Saleh M. Alrasheed (salrasheed@yahoo.com) Ibrahim A. Alorainy (ibrahimorainy@ksu.edu.sa) Lu M. Liu (tmbosley@bosleynet.net) John A. McGrath (Mcgrath@yahoo.com) Lionel M. Van ... Cited by 1 - Related articles - All 6 versions
K Naha, BA Shastry, K Saravu… - Australasian Medical Journal- …, 2011 - amj.net.au ...LipoidProteinosis Mimicking Congential Inmunodeficiency. Kushal Naha, B Ananthakrishna Shastry, Kavitha Saravu, Sumit Bhatia. Abstract. Lipoidproteinosis is a rare congenital disorder that can present with a variety of symptoms. ... Cached
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