International Journal of Pediatric Otorhinolaryngology Extra
Volume 6, Issue 4 , Pages 175-177 , December 2011

Long-term follow-up of lipoid proteinosis laryngeal manifestations

Received 24 May 2010 ,Revised 30 June 2010 ,Accepted 3 July 2010.

References 

  1. Hamada T, McLean WH, Ramsay M, Ashton GH, Nanda A, Jenkins T, et al. Lipoid proteinosis maps to 1q21 and is caused by mutations in the extracellular matrix protein 1 gene (ECM1). Hum. Mol. Genet. 2002;11:833–840
  2. Siebenmann F. Über Mitbeteiligung der Schleimhaut bei allgemeiner Hyperkeratose der Haut. Arch. Laryngol. Rhinol. (Berl.). 1908;20:101–109
  3. Urbach E, Wiethe C. Lipoidosis cutis et mucosae. Virchows Arch. Pathol. Anat. 1929;273:285–319
  4. Al-Bitar Y, Samdani AJ. Lipoid proteinosis in two brothers with multiple organ involvement from Saudi Arabia. Int. J. Dermatol. 2004;43:360–361
  5. Savage MM, Crockett DM, McCabe BF. Lipoid proteinosis of the larynx: a cause of voice change in the infant and young child. Int. J. Pediatr. Otorhinolaryngol. 1988;15:33–38
  6. Harper JI, Duguid KP, Staughton RC, Moffat DA. Oropharyngeal and laryngeal lesions in lipoid proteinosis. J. Laryngol. Otol. 1983;9:877–880
  7. Hofer PA, Bergenholtz A. Oral manifestations in Urbach–Wiethe disease (lipoglycoproteinosis; lipoid proteinosis; hyalinosis cutis et mucosae). Odontol. Revy. 1975;26:39–57
  8. Kleinert R, Cervos-Navarro J, Kleinert G, Walter GF, Steiner H. Predominantly cerebral manifestation in Urbach–Wiethe syndrome (lipoid proteinosis cutis et mucosae): a clinical and pathomorphological study. Clin. Neuropathol. 1987;6:43–45

PII: S1871-4048(10)00053-5

doi: 10.1016/j.pedex.2010.07.003

International Journal of Pediatric Otorhinolaryngology Extra
Volume 6, Issue 4 , Pages 175-177 , December 2011

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