Identification of Osteogenesis Imperfecta Type VI: A First Case Report from a Pakistani Family
Asia Parveen, Amina Arif, Shafia Arshad, Muhammad Shafeeq Ur Rahman, Faheem Ahmed Siddiqui & Muhammad Awais · Journal of Pharmaceutical Research International · 2021
Background: Osteogenesis imperfecta type VI (OI type VI) is a rare autosomal recessive disease of bone mineralization characterized by multiple bone fractures after six months of age, without a history of other extra-skeletal complications. SERPINF1 (serpin inhibitor clade F1) is...
Open access
Research Article
10.9734/jpri/2021/v33i60B34910