Osteogenesis imperfecta type
An X-linked recessive sub-type of osteogenesis imperfecta caused by mutation(s) in the MBTPS2 gene, encoding membrane-bound transcription factor site-2 protease. It is characterized by prenatal fractures and osteopenia, with severe short stature in adulthood. Variable dysmorphic features may occur including scoliosis, pectal deformity, and anterior angulation of the tibia.
Disease Alternative Name
Rachana Hospital
Director
Seth GSMC AND KEMH
MD DNB DCH
Gennextpolyclinic.com/blog and Others
20 Yrs Post Md Experience. Md .mrcpch(london) Pediatric Consultant .ranchi.jharkhand.
Mbbs Rims.ranchi Md.pmch.patna. Mrcpch (london)
mbbs.md.mrcpch.
Adichunchanagiri Institute of Medical Sciences
MBBS
ESIC , Gulbarga
MD General medicine
Senior Consultant Internal Medicine & Critical Care, Program Director for DNB Internal Medicine.
Mediciti Hospital
Southern Illinois University School Of Medicine
MD
Sepuri Endocrine & Diabetes Center
Chief Endocrinologist & Diabetologist for the Last 25 Years
Royal College of Physicians, United Kingdom
Masters Degree in Clinical Endocrinology & Diabetes
Myh
Intern
Mahatma Gandhi Memorial Medical College
MBBS
Emergency Medical Officer
Thane
Muhs
BAMS MD (BALROG)
Sree Rheumatic Centre
Consultant
Kurnool Medical College
MD- General Medicine
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