A Rare Case: Pseudohypoaldosteronism in the Neonatal Period
نویسندگان
چکیده
منابع مشابه
A Rare Case of Neonatal Hypophosphatasia: A Case Report
Hypophosphatasia is a rare hereditary disorder of bone metabolism.In this article, we presented the case of a male infant with a soft skull and short, deformed limbs at birth, followed by seizures and respiratory distress during admission in the neonatal intensive care unit (NICU). Prenatal ultrasound showed limb hypoplasia, skull hypomineralization, and polyhydramnios. Seizures occurred on day...
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A four day old female infant was admitted because of poor feeding, vomiting and jaundice. Laboratory examination showed hyperkalemia, mild hyponatremia and renal tubular acidosis type 4. Serum aldosterone and plasma renin activity were elevated but serum cortisol, 17 -hydroxyprogesterone, ACTH, 24 hour urinary 17- ketoste roid, pregnanetriol, renal function and sonogram were normal and henc...
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15 صفحه اولA Rare Case of Neonatal Birth with Congenital Bilateral Femoral Deficiency Undetected in Prenatal Ultrasound
Background:Prenatal ultrasound plays an important role in the early and accurate evaluation of the congenital skeletal and non-skeletal abnormalities of the fetus and is effective in predicting pregnancy outcomes. Congenital femoral deficiency (CFD) is a rare complicated and non-hereditary anomaly that includes the hypoplasia of a portion of the femoral bone with shortening the lower limb. Cas...
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Mucormycosis of the neonatal gut is a rare disease, with uniformly fatal prognosis. It has occasionally been reported involving the stomach and ileum in immunocompromised hosts. However, mucormycosis of the colon is very rare. We report case of a preterm, low birth weight (LBW) neonate with clinical features of Necrotising enterocolitis found to have characteristic black-velvety colonic gangren...
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ژورنال
عنوان ژورنال: Turkish Journal of Pediatric Disease
سال: 2016
ISSN: 1307-4490,2148-3566
DOI: 10.12956/tjpd.2016.215