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

Pediatric Dermatology

Volumn 19, Issue 4, 2002, Pages 317-319

  Urbatsch, Amy ^a,c   Paller, Amy S ^b  

^a UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

^b NORTHWESTERN UNIVERSITY MEDICAL CENTER   (United States)

^c NONE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MINERALOCORTICOID;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; DISEASE ASSOCIATION; HUMAN; HYDRAMNIOS; HYPONATREMIA; INFANT; INFLAMMATION; MALE; METABOLIC ACIDOSIS; PRIORITY JOURNAL; PSEUDOHYPOALDOSTERONISM; PUSTULOSIS; SALT LOSING NEPHRITIS; SKIN DISEASE; SODIUM RETENTION; SWEAT GLAND DISEASE;

DISEASE PROGRESSION; HUMANS; INFANT; MALE; MILIARIA; PROGNOSIS; PSEUDOHYPOALDOSTERONISM; RECURRENCE; RISK ASSESSMENT; SEVERITY OF ILLNESS INDEX; WATER-ELECTROLYTE IMBALANCE;

EID: 0036657049     PISSN: 07368046     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1525-1470.2002.00090.x     Document Type: Article

References (10)

1. Type I pseudohypoaldosteronism includes two clinically and genetically distinct entities with either renal or multiple target organ defects
2. Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalemic acidosis, pseudohypoaldosteronism type 1
3. Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type 1
4. Polyhydramnios as a sign of fetal pseudohypoaldosteronism
5. Pseudohypoaldosteronism with elevated sweat and saliva electrolyte value and frequent lower respiratory tract infections mimicking cystic fibrosis
6. Recurrent Pseudomonas bronchopneumonia in a child with type I pseudohypoaldosteronism
7. Pseudohypoaldosteronism: Options for consideration
8. Sweat glands in pseudohypoaldosteronism
9. Sweat chloride concentrations in infants homozygous or heterozygous for F508 cystic fibrosis
10. Pseudohypoaldosteronism due to sweat gland dysfunction