Literature DB >> 15533571

Lipoid proteinosis of larynx: review of four cases.

Aydin Acar1, Adil Eryilmaz, Celil Gocer, Halit Akmansu, Hakan Korkmaz.   

Abstract

Lipoid proteinosis is a rare autosomal recessive disorder characterized by intercellular deposition of an amorphous hyaline material. It mainly involves skin and mucosal membranes of upper aerodigestive tract as well as central nervous system, lung, lymph nodes and striated muscles. Etiology and pathogenesis are unknown. Infantile hoarseness is a common presenting feature of the disease due to infiltration of larynx. In two-thirds of the cases, voice changes are present at birth or in early infancy as the first manifestation. We present four patients with lipoid proteinosis involving skin, oropharynx and larynx.

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Year:  2004        PMID: 15533571     DOI: 10.1016/j.ijporl.2004.07.012

Source DB:  PubMed          Journal:  Int J Pediatr Otorhinolaryngol        ISSN: 0165-5876            Impact factor:   1.675


  3 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.  Amygdalae and striatum calcification in lipoid proteinosis.

Authors:  F G Gonçalves; M B de Melo; V de L Matos; F R Barra; R E Figueroa
Journal:  AJNR Am J Neuroradiol       Date:  2009-08-20       Impact factor: 3.825

3.  Radiologic presentation of lipoid proteinosis with symmetrical medial temporal lobe calcifications.

Authors:  Subhashree Chandrasekaran; Murali Nanjundan; Sundari Natarajan; Kannadhasan Ramadhas
Journal:  Radiol Case Rep       Date:  2016-02-17
  3 in total

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