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Challenges in the diagnosis and management of Pseudohypoaldosteronism Type 1
International Journal of Pediatric Endocrinology volume 2015, Article number: P126 (2015)
Autosomal recessive Pseudohypoaldosteronism Type I (PHA-I, MIM#264350), is a rare disease with a severe clinical phenotype [1, 2] and generally no improvement with age . It results from mutations in the amiloride-sensitive epithelial sodium channel causing mineralocorticoid-resistant (ENaC), systemic salt wasting, and is lethal without ongoing supra-physiological sodium supplementation and management of hyperkalaemia [4, 5].
Other manifestations of systemic PHA-I include decreased sodium-dependant clearance of alveolar fluid causing recurrent chest congestion, cough and wheeze, but no airway infection by bacterial pathogens typifying cystic fibrosis[6, 7]; and skin rashes from inflammation of sodium-blocked sweat glands  with recurrent Staphylococcal skin infections described .
Our patient, now nearly four years old, presented as a day 6 neonate with vomiting, apnoea and floppiness. She was shocked and dehydrated with hyponatraemia, marked hyperkalaemia with runs of ventricular tachycardia.
PHA-1 was diagnosed with high cortisol, renin and aldosterone, normal 17-hydroxyprogesterone, inappropriately high spot urine sodium with low potassium, and normal renal ultrasound. Diagnosis was genetically confirmed with the finding of two inherited, distinct, disease causing mutations in the SCNNIA gene. Increased sweat sodium confirmed systemic salt-wasting. Initial management included a high-sodium, low-potassium formula (Kindergen) supplemented with 22 mmol/Kg/day of enteral sodium, the use of daily potassium binding resin (Resonium), and trial of Fludrocortisone.
Requirement for daily large doses of sodium 16 mmol/Kg/day, provided as a mix of sodium citrate and sodium chloride, and daily Resonium continues. Significant oral aversion remains an issue with good growth achieved on calorie-concentrated Kindergen. Gastrostomy feeding was changed to percutaneous jejunal continual feeding due to persistent gastric emptying problems. Central venous access established early has posed ongoing challenges, with intermittent Staphylococcal infections. Our patient has also been hypertensive requiring medical management from 6 months age. She has a recurrent moist cough with past Haemophilus infection.
Minimising inpatient management is vital for establishing 'normality' and optimising development. The need for frequent electrolyte monitoring and adjustment of sodium intake is managed creatively between home and hospital in close liaison with her paediatric endocrinologist and community-based supports. Clear emergency management plans involving early symptom recognition and rapid hospital-access are instituted to manage salt-wasting episodes.
We shall discuss the challenges and pitfalls of managing this rare, life-threatening disease with sparse long-term prognostic information, in the Australian health care context.
Written informed consent was obtained from the parent of the patient for publication of this abstract and any accompanying images. A copy of the written consent is available for review by the Editor of this journal.
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Visser, U., Jenkins, P. & Lafferty, T. Challenges in the diagnosis and management of Pseudohypoaldosteronism Type 1. Int J Pediatr Endocrinol 2015, P126 (2015). https://doi.org/10.1186/1687-9856-2015-S1-P126
- Epithelial Sodium Channel
- Severe Clinical Phenotype
- Sweat Sodium
- Emptying Problem