Abstract
A new-born baby with Beckwith's syndrome had severe hypoglycaemia, and was treated with glucagon and prednisone. Treatment was stopped at 1 month of age and his blood glucose levels were satisfactory for the ensuing 6 weeks. However, at 10 weeks of age, he had a hypoglycaemic convulsion and required large doses of diazoxide and prednisone for the next 2 months to maintain the blood glucose above 40 mg/100 ml. Insulin excretion was raised until he was 4 months old. Cases of Beckwith's syndrome which develop hypoglycaemia, should be treated with diazoxide and corticosteroids until insulin excretion is normal.
Cite
CITATION STYLE
Moncrieff, M. W., Lacey, K. A., & Malleson, P. N. (1977). Management of prolonged hypoglycaemia in Beckwith’s syndrome. Postgraduate Medical Journal, 53(617), 159–161. https://doi.org/10.1136/pgmj.53.617.159
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