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 |
|---|---|
| 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
- General Medicine
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