Počet záznamov: 1
pemfigus benígny familiárny
SYS d016506 LBL 00000cx--j2200000---45-- 005 20240119200136.1 100 $a 19920103asloy0103----ba0 152 $b mesh 250 $a pemfigus benígny familiárny $x BL $x CF $x CI $x CL $x CO $x DG $x DH $x DI $x DT $x EC $x EH $x EM $x EN $x EP $x ET $x GE $x HI $x IM $x ME $x MI $x MO $x NU $x PA $x PC $x PP $x PS $x PX $x RH $x RT $x SU $x TH $x UR $x VE $x VI $8 slo 300 1-
$a 92 $8 eng 300 1-
$a Pemphigus (1966-1991) $8 eng 330 1-
$a An autosomal dominantly inherited skin disorder characterized by recurrent eruptions of vesicles and BULLAE mainly on the neck, axillae, and groin. Mutations in the ATP2C1 gene (encoding the secretory pathway Ca2++/Mn2++ ATPase 1 (SPCA1)) cause this disease. It is clinically and histologically similar to DARIER DISEASE - both have abnormal, unstable DESMOSOMES between KERATINOCYTES and defective CALCIUM-TRANSPORTING ATPASES. It is unrelated to PEMPHIGUS VULGARIS though it closely resembles that disease. $8 eng 450 $a Chronic Benign Familial Pemphigus $5 e $8 eng 450 $a Familial Benign Chronic Pemphigus $5 e $8 eng 450 $a Hailey-Hailey Disease $5 e $8 eng 450 $a pemfigus benígny chronický $5 e $8 slo 450 $a pemfigus benígny familiárny chronický $5 e $8 slo 450 $a Haileyova-Haileyova choroba $5 e $8 slo 450 $a Hailey-Haileyova choroba $5 e $8 slo 686 $a C16.320.850.700 686 $a C17.800.827.700 686 $a C17.800.865.858 750 $a Pemphigus, Benign Familial $8 eng 801 -0
$a US $b DNLM $c 19920103 801 -2
$a SK $b BA006 $c 20070706 801 -2
$a SK $b BA006 $c 20110510 801 -2
$a SK $b BA006 $c 20201119 980 $x M
Počet záznamov: 1