Atrichia With Papular Lesions
Watchlist
Retrieved
2021-01-23
Source
Trials
—
Genes
HR,
ODC1,
RARA,
PML,
ZBTB16,
PRAM1,
FLT3,
NPM1,
DAPK2,
TRIB3,
AS3MT,
PPARG,
ADCY9,
SQSTM1,
VDR,
VAV1,
ATG5,
TWIST1,
TSHR,
TP73,
TOP2B,
CCNA1,
KHDRBS1,
ZMPSTE24,
AGPAT2,
TACR1,
RAB40B,
PEG10,
NUP62,
DCTN4
HR,
ODC1,
RARA,
PML,
ZBTB16,
PRAM1,
FLT3,
NPM1,
DAPK2,
TRIB3,
AS3MT,
PPARG,
ADCY9,
SQSTM1,
VDR,
VAV1,
ATG5,
TWIST1,
TSHR,
TP73,
TOP2B,
CCNA1,
KHDRBS1,
ZMPSTE24,
AGPAT2,
TACR1,
RAB40B,
PEG10,
NUP62,
DCTN4,
LEF1,
KDM3B,
LMNB2,
PRRT2,
NEAT1,
MIR181A2,
MIR17HG,
TRBV20OR9-2,
MAPK3,
RXRA,
FGFR1,
AKT1,
ANXA5,
APRT,
FAS,
CEBPB,
CEBPE,
DAP,
F2,
F2RL1,
F3,
PTK2B,
FANCB,
FGF13,
KAT2A,
AGL,
GTF2H1,
HLA-DRB1,
HOXB2,
ITGAM,
LMNA,
MATN1,
MFAP1,
MYC,
NCAM1,
PRF1,
PRKAR1A,
PRKCA,
PRKCB,
BCRP3
Drugs
—
Registered!
A rare inherited form of alopecia characterized by irreversible hair loss during the neonatal period on all hear-bearing areas of the body, later associated with the development of papular lesions all over the body and preferentially on the face and extensor surfaces of the extremities.