Lamellar Ichthyosis is a rare genodermatotic condition, which occurs due to the mutation in the transglutaminase- 1gene. It is a rare disease with a global prevalence of 1 in 300000 live births with no specific gender predilection. It is a rare genetic disorder with a characteristic fish scale appearance of the skin. Here we report one such rare case of Lamellar Ichthyosis in a 7- year-old girl reported to us with difficulty in chewing.

Original languageEnglish
Pages (from-to)121-124
Number of pages4
JournalJournal of Krishna Institute of Medical Sciences University
Issue number3
Publication statusPublished - 01-01-2019

All Science Journal Classification (ASJC) codes

  • Medicine(all)


Dive into the research topics of 'Lamellar ichthyosis: A rare mucocutaneous disease'. Together they form a unique fingerprint.

Cite this