Pustular miliaria rubra: A specific cutaneous finding of type I pseudohypoaldosteronism

被引:17
|
作者
Urbatsch, A
Paller, AS
机构
[1] Univ Alabama, Dept Dermatol, Birmingham, AL 35294 USA
[2] Northwestern Univ, Dept Pediat Dermatol, Med Ctr, Chicago, IL 60611 USA
关键词
D O I
10.1046/j.1525-1470.2002.00090.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Type I pseudohypoaldosteronism, an autosomal recessive, life-threatening disorder of mineralocorticoid resistance leads to excessive loss of sodium chloride through eccrine and other secretions. Recurrent episodes of pustular miliaria rubra are associated with salt-losing crises and clear spontaneously with stabilization. Inflammation of and around the damaged eccrine glands has been attributed to the deleterious effects of excessive eccrine gland salt exposure.
引用
收藏
页码:317 / 319
页数:3
相关论文
共 50 条
  • [21] Phenotypic variation of autosomal recessive pseudohypoaldosteronism type I: a case in point
    Ahluwalia, Gunjeet Kala
    Dasouki, Majed
    Lennon, Angela
    CLINICAL CASE REPORTS, 2014, 2 (06): : 326 - 330
  • [22] Pseudohypoaldosteronism type I Rare differential diagnosis in a newborn with feeding difficulties
    Mezger, A.
    Ruland, A.
    Ruef, P.
    MONATSSCHRIFT KINDERHEILKUNDE, 2022, 170 (03) : 257 - 260
  • [23] Heterozygous β epithelial sodium channel mice exhibit features of pseudohypoaldosteronism type I (PHA I).
    Williamson, RA
    Yang, B
    Cao, XR
    Welsh, MJ
    Stokes, JB
    AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 606 - 606
  • [24] PSEUDOHYPOALDOSTERONISM - EVALUATION OF TYPE-I RECEPTORS BY RADIORECEPTOR ASSAY AND BY ANTIRECEPTOR ANTIBODIES
    ARMANINI, D
    KARBOWIAK, I
    ZENNARO, CM
    ZOVATO, S
    PRATESI, C
    DELAZZARI, P
    KROZOWSKI, Z
    KUHNLE, U
    STEROIDS, 1995, 60 (01) : 161 - 163
  • [25] Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I
    Geller, DS
    Rodriguez-Soriano, J
    Boado, AV
    Schifter, S
    Bayer, M
    Chang, SS
    Lifton, RP
    NATURE GENETICS, 1998, 19 (03) : 279 - 281
  • [26] Chronic Pseudomonas colonization of the skin, ear and eyes in a child with type I pseudohypoaldosteronism
    Garty, BZ
    ACTA PAEDIATRICA, 1999, 88 (04) : 472 - 473
  • [27] Refractory Type I pityriasis rubra pilaris treated with tildrakizumab
    Licata, G.
    Gambardella, A.
    Calabrese, G.
    Pagliuca, F.
    Alfano, R.
    Argenziano, G.
    CLINICAL AND EXPERIMENTAL DERMATOLOGY, 2021, 46 (08) : 1594 - 1595
  • [28] Treatment of pityriasis rubra pilaris type I: a systematic review
    Engelmann, Carina
    Elsner, Peter
    Miguel, Diana
    EUROPEAN JOURNAL OF DERMATOLOGY, 2019, 29 (05) : 524 - 537
  • [29] Treatment of pityriasis rubra pilaris type I: a systematic review
    Carina Engelmann
    Peter Elsner
    Diana Miguel
    European Journal of Dermatology, 2019, 29 : 524 - 537
  • [30] Successful use of etanercept in type I pityriasis rubra pilaris
    Seckin, D.
    Tula, E.
    Ergun, T.
    BRITISH JOURNAL OF DERMATOLOGY, 2008, 158 (03) : 642 - 644