Mild lamellar ichthyosis with a truncated homozygous TGM1 mutation in a pediatric patient from Turkey
Dermatol Ther
.
2020 Nov;33(6):e14152.
doi: 10.1111/dth.14152.
Epub 2020 Sep 6.
Authors
Işıl Göğem İmren
1
,
Efsun Tanacan
2
,
Serdar Ceylaner
3
,
Gokce Sumer
4
,
Meral Eksioglu
5
Affiliations
1
Department of Dermatology, Faculty of Medicine, Pamukkale University, Denizli, Turkey.
2
Department of Dermatology, Ufuk University, Ankara, Turkey.
3
Department of Medical Genetics, İntergen Genetic Diagnosis and Research Center, Ankara, Turkey.
4
Department of Pediatrics, University of Health Sciences Ankara Research and Training Hospital, Ankara, Turkey.
5
Department of Dermatology, University of Health Sciences Ankara Research and Training Hospital, Ankara, Turkey.
PMID:
32767474
DOI:
10.1111/dth.14152
No abstract available
Publication types
Letter
MeSH terms
Child
Homozygote
Humans
Ichthyosis, Lamellar* / diagnosis
Ichthyosis, Lamellar* / genetics
Mutation
Turkey