Isolated congenital growth hormone deficiency. Severe hypoglycemia and neonatal giant cell hepatitis
作者： Jacobsen Bb , Esberg Bh
DOI:
关键词: Internal medicine 、 Congenital Growth Hormone Deficiency 、 Hypoplasia 、 Endocrinology 、 Severe hypoglycemia 、 Pituitary gland 、 Medicine 、 Substitution therapy 、 Failure to thrive 、 Neonatal giant cell hepatitis 、 Jaundice
摘要: A case of congenital isolated growth hormone deficiency with neonatal giant cell hepatitis is described. Hypoplasia the pituitary gland was detected by a MR-scan. Values IGF-I, IGF-II, and IGF-BP-3 were low. Birth length weight normal; hypoglycaemia, jaundice, failure to thrive most pronounced symptoms present from first day. Substitution therapy induced remission all symptoms. Growth normal at follow-up age two half years.
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