heterozygous or homozygous variety, which leads to the expression of lamellarichthyosis as a result of abnormal cross-linkaging of the cornified cell envelope
Recessive loss-of-function mutations in TGM1 have been shown to cause lamellarichthyosis, a disease characterized by excessive scaling and shedding of the
describe a certain type of ichthyosis, a congenital skin condition. LamellarIchthyosis often presents with a "colloidal" membrane at birth. It is characterized
"Oral liarozole in the treatment of patients with moderate/severe lamellarichthyosis: Results of a randomized, double-blind, multinational, placebo-controlled
Ruiz-Maldonado, R. (1980). "Oral retinoid (Ro 10-9359) in children with lamellarichthyosis, epidermolytic hyperkeratosis and symmetrical progressive erythrokeratoderma"
differentiation of keratinocytes. Mutations in this gene are associated with lamellarichthyosis type 4. [provided by RefSeq, Dec 2011]. GRCh38: Ensembl release 89:
(November–December 2017). "Psedoanihum and autoamputation associated with lamellarichthyosis". Indian Journal of Dermatology, Venereology and Leprology: 728.{{cite
Inactivating mutations in ALOX3 are also associated with the human disease lamellarichthyosis (see Ichthyosis § Types – item 5 in the table). Two lipoxygenases
sometimes used, but may be considered offensive when applied to people). Lamellarichthyosis, also called "fish scale disease", is an inherited condition in which
(November 1996). "Corrective gene transfer in the human skin disorder lamellarichthyosis". Nature Medicine. 2 (11): 1263–1267. doi:10.1038/nm1196-1263. PMID 8898758