hrp0086p2-p592 | Perinatal Endocrinology P2 | ESPE2016
Alghazir Nadia
, Gadaffi Omalmir
, Hadeed Ibtisam
, Abusrewil Suliman
, Doggah Milad
, Guail Milad
Background: Neonatal hyperparathyrodisim can be caused by homozygous and heterozygous inactivating mutation in the calcium-sensing receptor can cause familial hypocalciuric hypercalcaemia (FHH) or neonatal sever hyperparathyroidism (NSHPTT). NSHPT represents the most sever expression of FHH and courses as life threatening condition.Objective and hypotheses: Neonatal hyperparathyrodisim can be caused by homozygous and heterozygous inactivating mutation in...