Osteogenesis imperfecta is a genetic condition with improperly or inadequately produced Type I collagen. Manifestations include bowing deformities, fractures, hydrocephalus, respiratory insufficiency, and feeding difficulty. Moderate or severe OI is often diagnosed prenatally based on ultrasound findings and ...
Where is osteogenesis imperfecta most common? What are the different types of interstitial lung disease? What is the medical term for normal breathing? How many people have mesothelioma? What is chronic pulmonary thromboembolic disease? What is a chronic respiratory disease arising in the perinatal pe...
Based on our calculations, we deduce that the HgACBP–membrane interaction occurs through a protein–membrane orientation common to neutral and negatively charged membranes. Moreover, our electrostatic model on the HgACBP–membrane system shows that the protein interaction with anionic phospholipid-rich ...
and most painful(痛苦的) decision in our life.Our five-week-old daughter,Alle Shea,was born with osteogenesis imperfecta (成骨不全症).The day Alle was leaving us,we took her out of the hospital and held her in our arms (3) A
Guillain-Barre syndrome can affect all age groups, but the risk increases with age. Guillain-Barre syndrome is most common in males over the age of...Become a member and unlock all Study Answers Start today. Try it now Create an account Ask a question Our experts can answer your ...
(1989) Type I procollagen: the gene-protein system that harbors most of the mutations causing osteogenesis imperfecta and probably more common heritable disorders of connective tissue. Am J Med Genet 34: 60–67Prockop, D.J., Constantinou, C.D., Dombrowski, K.E., Hojima, Y., Kadler, K...
Genotype and phenotype correlation ofWNT1mutations has not been established. Here we present two female siblings with osteogenesis imperfecta (OI) born to a consanguineous couple. Both sustained severe bone deformities. However, only the younger had severe brain anomalies resulting in an early death ...