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Microcephalic osteodysplastic primordial dwarfism type I (MOPD I) is a rare autosomal recessive developmental disorder characterized by extreme intrauterine growth ation, severe microcephaly, central nervous system abnormalities, dysmorphic facial features, skin abnormalities, skeletal changes, limb deformations,
Medicine. Medical Outpatients Department (MOPD)
Microcephalic osteodysplastic primordial dwarfism (MOPD) is a syndrome characterized by the presence of intrauterine growth restriction, post-natal growth deficiency, microcephaly and a similar phenotype to Seckel syndrome.