spondyloepiphyseal dysplasia การใช้

• It is similar, if not identical, to Spondyloepiphyseal Dysplasia Tarda in humans.
• The signs and symptoms of this condition at birth are very similar to those of spondyloepiphyseal dysplasia congenita, a related skeletal disorder.
• There is an identical issue at Spondyloepiphyseal dysplasia congenita, so whatever is decided about the first page should apply to this one as well.
• Pseudoachondroplasia ( also known as PSACH, Pseudoachondroplastic dysplasia, and Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome ) is an osteochondrodysplasia that results in mild to severely short stature due to the inhibition of skeletal growth primarily in the limbs ( COMP 2008 ).
• Features of Stickler syndrome type II include : sensorineural hearing loss, facial features ( flat facial profile, anteverted nares, micrognathia ), cleft palate, visual disturbances ( type 2 vitreous anomaly, childhood-onset myopia, glaucoma, cataracts and retinal detachment ), spondyloepiphyseal dysplasia, and arthropathy.
• Thirteen other syndromes may exhibit signs similar to Usher syndrome, including Alport syndrome, Alstrom syndrome, Bardet-Biedl syndrome, Cockayne syndrome, spondyloepiphyseal dysplasia congenita, Flynn-Aird syndrome, Friedreich ataxia, Hurler syndrome ( MPS-1 ), Kearns-Sayre syndrome ( CPEO ), Norrie syndrome, osteopetrosis ( Albers-Schonberg disease ), Refsum's disease ( phytanic acid storage disease ), and Zellweger syndrome ( cerebrohepatorenal syndrome ).