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
  • [31] Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I
    David S. Geller
    Juan Rodriguez-Soriano
    Alfredo V. Boado
    Søren Schifter
    Milan Bayer
    Sue S. Chang
    Richard P. Lifton
    Nature Genetics, 1998, 19 : 279 - 281
  • [32] A PARTIAL FORM OF PSEUDOHYPOALDOSTERONISM TYPE-I WITHOUT RENAL SODIUM WASTING
    BALLAUFF, A
    WENDEL, U
    KUPKE, I
    KUHNLE, U
    JOURNAL OF PEDIATRIC ENDOCRINOLOGY, 1994, 7 (01) : 57 - 60
  • [33] Different inactivating mutations of the mineralocorticoid receptor in fourteen families affected by type I pseudohypoaldosteronism
    Sartorato, P
    Lapeyraque, AL
    Armanini, D
    Kuhnle, U
    Khaldi, Y
    Salomon, R
    Abadie, R
    Di Battista, E
    Naselli, A
    Racine, A
    Bosio, M
    Caprio, M
    Poulet-Young, V
    Chabrolle, JP
    Niaudet, P
    De Gennes, C
    Lecornec, MH
    Poisson, E
    Fusco, AM
    Loli, P
    Lombès, M
    Zennaro, MC
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (06): : 2508 - 2517
  • [34] Recurrent Pseudomonas bronchopneumonia and other symptoms as in cystic fibrosis in a child with type I pseudohypoaldosteronism
    Marthinsen, L
    Kornfält, R
    Aili, M
    Andersson, D
    Westgren, U
    Schaedel, C
    ACTA PAEDIATRICA, 1998, 87 (04) : 472 - 474
  • [35] Nevus Anemicus: A Distinctive Cutaneous Finding in Neurofibromatosis Type 1
    Hernandez-Martin, Angela
    Javier Garcia-Martinez, Francisco
    Duat, Anna
    Lopez-Martin, Inmaculada
    Noguera-Morel, Lucero
    Torrelo, Antonio
    PEDIATRIC DERMATOLOGY, 2015, 32 (03) : 342 - 347
  • [36] Successful treatment of refractory type I pityriasis rubra pilaris with ustekinumab
    Allen, N.
    Smith, A.
    AUSTRALASIAN JOURNAL OF DERMATOLOGY, 2021, 62 : 21 - 21
  • [37] Type I and type III collagens in cutaneous mucinosis
    Alves, MFGS
    Filgueira, AL
    Lorena, DE
    Porto, LC
    AMERICAN JOURNAL OF DERMATOPATHOLOGY, 1998, 20 (01) : 41 - 47
  • [38] Scarring Alopecia in Classic Adult Type I Pityriasis Rubra Pilaris
    Martin Callizo, C.
    Molinero Caturla, J.
    Sanchez Sanchez, J.
    Penin Mosquera, R. M.
    ACTAS DERMO-SIFILIOGRAFICAS, 2014, 105 (10): : 955 - 957
  • [39] A patient presenting with nail changes and type I pityriasis rubra pilaris
    Santoro, Frank
    Nallamothu, Padma
    JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2012, 66 (04) : AB96 - AB96
  • [40] Autosomal recessive pseudohypoaldosteronism type I (PHA-I) with congenital glaucoma & diminished immunoglobulins: Expanding the phenotype.
    Schwartz, ID
    Jacobson, JD
    PEDIATRIC RESEARCH, 1996, 39 (04) : 577 - 577