Cutaneous and Ocular Findings in Systemic Pseudohypoaldosteronism I: Early Clinical Pointers

Systemic Pseudohypoaldosteronism type I (PHA I) is an uncommon and an often missed cause of salt wasting crisis in the neonatal period. In addition to dyselectrolytemia, cutaneous findings in the form of miliaria rubra, and ophthalmic findings secondary to abnormal sebum accumulation in the eye may...

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Main Authors: Neha Agarwal (Author), Alpa Gupta (Author), Renu Dhasmana (Author), Ashima Mehta (Author), Nitika Agrawal (Author)
Format: Book
Published: JCDR Research and Publications Pvt. Ltd., 2022-03-01T00:00:00Z.
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100 1 0 |a Neha Agarwal  |e author 
700 1 0 |a Alpa Gupta  |e author 
700 1 0 |a Renu Dhasmana  |e author 
700 1 0 |a Ashima Mehta  |e author 
700 1 0 |a Nitika Agrawal  |e author 
245 0 0 |a Cutaneous and Ocular Findings in Systemic Pseudohypoaldosteronism I: Early Clinical Pointers 
260 |b JCDR Research and Publications Pvt. Ltd.,   |c 2022-03-01T00:00:00Z. 
500 |a 10.7860/IJNMR/2022/50253.2324 
500 |a 2277-8527 
500 |a 2455-6890 
520 |a Systemic Pseudohypoaldosteronism type I (PHA I) is an uncommon and an often missed cause of salt wasting crisis in the neonatal period. In addition to dyselectrolytemia, cutaneous findings in the form of miliaria rubra, and ophthalmic findings secondary to abnormal sebum accumulation in the eye may also be present in patients with systemic PHA I. This article is about systemic PHA in a female neonate (birth weight 2.040 Kg, delivered at 34 weeks of gestation), who presented with life-threatening hyperkalemia, along with characteristic cutaneous and ophthalmic manifestations. Normal female genitalia, history of hyperkalemia with similar cutaneous and ophthalmic manifestations leading to death in the previous sibling, provided clue to the diagnosis. All relevant investigations were performed. Blood chemistry in this neonate revealed hyponatremia and hyperkalemia with metabolic acidosis. Plasma renin and serum aldosterone levels were reportedly high. Neonate was followed and electrolytes were monitored twice weekly on outpatient basis. But the life-threatening hyperkalemia led to multiple episodes of vomiting and, refusal to feed for few hours and the baby succumbed to death at age of 2.5 months. Hence, it was concluded that systemic PHA I should be considered in the differential diagnosis of neonates presenting with hyponatremic dehydration, hyperkalemia, and metabolic acidosis. Timely and appropriate electrolyte correction is pivotal for favourable outcome. 
546 |a EN 
690 |a hyperkalemia 
690 |a neonate 
690 |a salt wasting crisis 
690 |a Medicine 
690 |a R 
690 |a Pediatrics 
690 |a RJ1-570 
655 7 |a article  |2 local 
786 0 |n Indian Journal of Neonatal Medicine and Research, Vol 10, Iss 01, Pp 04-06 (2022) 
787 0 |n https://www.ijnmr.net/articles/PDF/2324/50253_CE[Ra1]_F(SHU)_PF1(AKA_SHU)_PFA(SHU)_PN(SHU).pdf 
787 0 |n https://doaj.org/toc/2277-8527 
787 0 |n https://doaj.org/toc/2455-6890 
856 4 1 |u https://doaj.org/article/73f58d37a7fc4a34bca6a9de908046ee  |z Connect to this object online.