RADOIR NEWS – The number of rare diseases approved at RADOIR’s medical committee raised to 248 by Dec. 2018.
RADOIR medical committee members as prof. Farhoud, Dr. Hamidreza Edraki, Dr. Mehdi Norouzi, and Dr. Saideh Mahdipour declared approval of:
2-hydroxyglutaric aciduria, Cerebral dysgenesis, Churg-Strauss syndrome(Eosinophilic granulomatosis with polyangiitis), Congenital myopathy, Dejerine-Sottas syndrome(Charcot-Marie-Tooth disease type 3), Gelatinous drop-like corneal dystrophy(GDCD), Glutaric aciduria, Hennekam syndrome, Idiopathic juvenile osteoporosis, Isolated growth hormone deficiency, Isovaleric academia, Oromandibular dystonia, Papillon-Lefèvre syndrome, Familial isolated hypoparathyroidism due to agenesis of parathyroid gland, Prion Infection, Seckel syndrome, Single Ventricle Defects, Succinic semialdehyde dehydrogenase deficiency( 4-Hydroxybutyric Aciduria), Tricuspid atresia.
The medical committee has started since the beginning of 2018 at which the patients’ files are revised and discussed every two weeks.
