Ichthyosis Linearis Circumflexa
Watchlist
Retrieved
2021-01-18
Source
Trials
—
Genes
SPINK5,
ST14,
KLK5,
KLK7,
FLG,
DSG1,
ELANE,
NPHS1,
VEGFA,
NPHS2,
APP,
AVP,
BTD,
CDSN,
CCR5,
CTRL,
ACE,
DEFB4A,
DRD4,
EPO,
ERBB2,
FLNA,
GBA,
GBAP1,
GH1,
GPT,
GYPA,
GYPB,
GYPE,
HRAS
SPINK5,
ST14,
KLK5,
KLK7,
FLG,
DSG1,
ELANE,
NPHS1,
VEGFA,
NPHS2,
APP,
AVP,
BTD,
CDSN,
CCR5,
CTRL,
ACE,
DEFB4A,
DRD4,
EPO,
ERBB2,
FLNA,
GBA,
GBAP1,
GH1,
GPT,
GYPA,
GYPB,
GYPE,
HRAS,
ICAM1,
IFNG,
IL17A,
IVL,
KRAS,
MIF,
COX2,
PI3,
POU5F1,
KLK6,
PTH,
PTGS2,
PTPN11,
SPINK1,
STAT3,
TGM1,
TNF,
SOCS3,
SOCS5,
MERTK,
IVNS1ABP,
SUB1,
IL36B,
IGHV1-12,
ICOS,
KLK14,
IL22,
NLRX1,
IL33,
IL17F,
POU5F1P3,
POU5F1P4,
DEFB4B,
MTCO2P12
Registered!

Ichthyosis linearis circumflexa is a distinctive skin condition of generalized hyperkeratosis and polycyclic and serpiginous erythematous plaques with a characteristic, migratory, double-edged scale at the margins, and is the typical cutaneous manifestation of Netherton's syndrome.:496:563
See also
- Ichthyosis prematurity syndrome
- List of cutaneous conditions