hrp0086p1-p116 | Bone & Mineral Metabolism P1 | ESPE2016

Clinical and Molecular Characterization of 25-Hydroxylase Deficiency in Saudi Patients

Imtiaz Faiqa , Bakhamis Sarah , AlSagheir Osamah , AlRajhi Abdulrahman

Background: Vitamin-D deficiency becomes a worldwide issue, and major cause of rickets in younger age groups. Multiple causes lead to vitamin-D deficiency in which nutritional causes contribute the major factor. The synthesis of bioactive vitamin-D requires hydroxylation at 1α and 25 positions by cytochrome-P450 in the kidney and liver, respectively. Recently, human CYP2R1 has been reported as a major factor for 25-hydroxylation, in which it contributes for the inherited ...

hrp0084p2-520 | Pituitary | ESPE2015

Two Novel LHX3 Mutations in Patients with Combined Pituitary Hormone Deficiency and Sensorineural Hearing Loss

Bin-Abbas Bassam , Ramzan Khushnooda , Allam Rabab , Al-Owain Mohammed , Imtiaz Faiqa

Background: Pituitary hormone deficiency combined type 3 (CPHD3; MIM# 221750) is an autosomal recessive combined pituitary hormone deficiency caused by mutations in LHX3, a LIM-homeodomain transcription factor gene which is necessary for the normal pituitary and motorneuron development.Aims: Clinical manifestations of CPHD3 are pituitary dwarfism and might be accompanied by rigid cervical spine leading to limited neck rotation or sensorineural deafness. ...