Literature DB >> 11207965

Lipoid proteinosis: report of four siblings and brief review of the literature.

A Nanda1, Q A Alsaleh, H Al-Sabah, A M Ali, J T Anim.   

Abstract

Lipoid proteinosis (Urbach-Wiethe disease) is a rare autosomal recessive disorder associated with deposition of periodic acid-Schiff (PAS)-positive hyaline material in various tissues including skin, mucous membranes, and internal organs. A family is reported in which four siblings (two boys and two girls) born to nonconsanguineous parents had lipoid proteinosis. All had the characteristic hoarseness of voice and three had skin lesions. The diagnosis was confirmed by the presence of typical features on light and electron microscopy.

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Year:  2001        PMID: 11207965     DOI: 10.1046/j.1525-1470.2001.018001021.x

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN: 0736-8046            Impact factor:   1.588


  9 in total

Review 1.  Lipoid proteinosis of Urbach and Weithe: case report and a brief review of the literature.

Authors:  Monal P Sainani; R Muralidhar; K Parthiban; P Vijayalakshmi
Journal:  Int Ophthalmol       Date:  2011-01-26       Impact factor: 2.031

2.  Lipoid proteinosis mimicking congenital immunodeficiency: a case report.

Authors:  Kushal Naha; Ananthakrishna B Shastry; Kavitha Saravu; Sumit Bhatia
Journal:  Australas Med J       Date:  2011-03-31

3.  Lipoid Proteinosis in two Iranian Sisters: A Case Report and Review of Literature.

Authors:  F Malekzad; H Rahimi; S Lotfi; M Qaisari
Journal:  Iran Red Crescent Med J       Date:  2011-04-01       Impact factor: 0.611

4.  Lipoid proteinosis.

Authors:  Roopa Shamsundar Rao; Sunita S Betkerur; Chaitanya Babu; Vm Sudha
Journal:  J Oral Maxillofac Pathol       Date:  2009-07

5.  Lipoid proteinosis: A review with two case reports.

Authors:  Vishal Kabre; Smitha Rani; Keerthilatha M Pai; Sakshi Kamra
Journal:  Contemp Clin Dent       Date:  2015 Apr-Jun

6.  Lipoid proteinosis in a six-year-old child.

Authors:  Surajit Nayak; Basanti Acharjya
Journal:  Indian Dermatol Online J       Date:  2012-01

7.  Treatment of lipoid proteinosis due to the p.C220G mutation in ECM1, a major allele in Chinese patients.

Authors:  Rong Zhang; Yang Liu; Yang Xue; Yinan Wang; Xinwen Wang; Songtao Shi; Tao Cai; Qintao Wang
Journal:  J Transl Med       Date:  2014-04-04       Impact factor: 5.531

8.  Lipoid Proteinosis.

Authors:  Hitesh C Mittal; Sunil Yadav; Sunita Malik; Gurdarshan Singh
Journal:  Int J Clin Pediatr Dent       Date:  2016-06-15

9.  Intra-Familial Variability of Lipoid Proteinosis: An Indian Case Series.

Authors:  Kriti Lohia; Bhavana R Doshi; Nagbhushan S Chougule
Journal:  Indian J Dermatol       Date:  2021 Sep-Oct       Impact factor: 1.494

  9 in total

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