Nephrocalcinosis in Shwachman's syndrome.
نویسندگان
چکیده
منابع مشابه
Nephrocalcinosis in Shwachman's syndrome
pregnancy, labour, and delivery. He was initially fed orally on a standard infant formula, but feeding became increasingly difficult and he failed to thrive. At 6 weeks of age, he was admitted to hospital, where he continued to gain weight poorly despite numerous feed changes. Nasogastric feeding was therefore started at 10 weeks of age. Investigations showed intermittent neutropenia (the lowes...
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A 29-year-old woman presented with a known nephrocalcinosis that had developed nine years earlier. Her past medical history was remarkable for a cardiac arrest secondary to a profound hypokalaemia (1.7 mEq/L) in the post-operative period following a complicated appendicular peritonitis at 19 years of age. Her on-going treatment included potassium citrate supplementation and increased fluid inta...
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Familial Hypomagnesemia, Hypercalciuria with Nephrocalcinosis is a rare autosomal recessive inherited disease associated with renal failure. Two girls born of consanguineous parentage aged 16 and 17 presented to us with renal failure, nephrocalcinosis and bone deformities. On evaluation they were found to have hypomagnesemia, hypercalciuria, increased fractional excretion of magnesium, hypocitr...
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Figure 1 – Abdominal X-ray of the patient showing clustered calcifications in projection of the kidneys, more evident at the right side (upper arrow identifies one of these clusters). An 8-mm right distal ureteral stone is present (lower arrow). A 46-year-old white woman has been followed in this nephrology clinic since 1995 due to recurrent nephroli-thiasis and medullary nephrocalcinosis resul...
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ژورنال
عنوان ژورنال: Archives of Disease in Childhood
سال: 1989
ISSN: 0003-9888,1468-2044
DOI: 10.1136/adc.64.4.614