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Stiff person spectrum disorder diagnosis, misdiagnosis, and suggested diagnostic criteria.
Chia NH, McKeon A, Dalakas MC, Flanagan EP, Bower JH, Klassen BT, Dubey D, Zalewski NL, Duffy D, Pittock SJ, Zekeridou A. Chia NH, et al. Ann Clin Transl Neurol. 2023 Jul;10(7):1083-1094. doi: 10.1002/acn3.51791. Epub 2023 May 22. Ann Clin Transl Neurol. 2023. PMID: 37212351 Free PMC article.
SPSD more often had hypertonia (60% vs. 24%, p < 0.001), hyperreflexia (71% vs. 43%, p = 0.001), and lumbar hyperlordosis (67% vs. 9%, p < 0.001) and less likely functional neurologic signs (6% vs. 33%, p = 0.001). ...

SPSD more often had hypertonia (60% vs. 24%, p < 0.001), hyperreflexia (71% vs. 43%, p = 0.001), and lumbar hyperlordosis (

A narrative review on spinal deformities in people with cerebral palsy: Measurement, norm values, incidence, risk factors and treatment.
Britz E, Langerak NG, Lamberts RP. Britz E, et al. S Afr Med J. 2020 Jul 29;110(8):767-776. doi: 10.7196/SAMJ.2020.v110i8.14472. S Afr Med J. 2020. PMID: 32880305 Review.
There is especially a worry about the increase of scoliosis, thoracic hyperkyphosis, lumbar hyperlordosis, spondylolysis and spondylolisthesis incidence, though supporting literature is lacking. ...
There is especially a worry about the increase of scoliosis, thoracic hyperkyphosis, lumbar hyperlordosis, spondylolysis and s …
Height outcome of short children with hypochondroplasia after recombinant human growth hormone treatment: a meta-analysis.
Massart F, Miccoli M, Baggiani A, Bertelloni S. Massart F, et al. Pharmacogenomics. 2015 Nov;16(17):1965-73. doi: 10.2217/pgs.15.129. Epub 2015 Nov 10. Pharmacogenomics. 2015. PMID: 26555758
Hypochondroplasia (HCH) is a genetic skeletal dysplasia, characterized by rhizomelic short height (Ht) with facial dysmorphology and lumbar hyperlordosis. Albeit there are concerns that HCH children may not achieve optimal long-term outcome in response to recombinan …
Hypochondroplasia (HCH) is a genetic skeletal dysplasia, characterized by rhizomelic short height (Ht) with facial dysmorphology and lumb