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“idiom” : “iphone”,
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},
{
“idiom” : “iphone”,
“scale” : “2x”,
“filename” : “Menu@2x.png”
},
{
“idiom” : “iphone”,
“scale” : “3x”,
“filename” : “Menu@3x.png”
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],
“info” : {
“version” : 1,
“author” : “xcode”
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}Ostholstein-Kronach syndrome: a rare cause of neonatal hypoglycaemia and hypopituitarism.
In this case report we present a female patient with neonatal hypoglycaemia and hypopituitarism due to a congenital absence of the pituitary gland. Hypoglycaemia in the early neonatal period was related to rapid growth and may be due to the shortage of glucose in the liver. We call our patient Ostholstein-Kronach syndrome, i.e. hypoglycaemia associated with incomplete insular dysgenesis and hypothalamic hypoplasia. The absence of the pituitary gland causes growth retardation, hypoglycaemia and hypopituitarism. As a consequence of the hypoglycaemia, a special complex of biochemical disturbances develops, the severity of which is greatest during neonatal life. We conclude that patients with hypoglycaemia and incomplete insular dysgenesis should be treated
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