Abstract
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 language | English |
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Pages (from-to) | 121-124 |
Number of pages | 4 |
Journal | Journal of Krishna Institute of Medical Sciences University |
Volume | 8 |
Issue number | 3 |
Publication status | Published - 01-01-2019 |
All Science Journal Classification (ASJC) codes
- Medicine(all)