Spontaneous splenic rupture and factor VII deficiency in a child with Noonan syndrome
A 16-year-old male with Noonan Syndrome presented to a district general hospital with abdominal pain, jaundice and collapse. Admitting blood tests were as follows: haemoglobin of 11.5 g/L, lactate of 4.2 mmol/L, bilirubin of 69 µmol/L, ALP of 154 U/L, white cell count of 24.7x10^9/L and a deranged c...
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Format: | Book |
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Elsevier,
2018-11-01T00:00:00Z.
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A1234.567 |
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Copy 1 | Available |