Syringomyelia
What's New
Last Posted: Feb 27, 2023
- Frequency and characteristics of congenital intraspinal abnormalities in a cohort of 128 patients with congenital scoliosis.
Mariscal Gonzalo, et al. Journal of craniovertebral junction & spine 2020 0 (4) 229-233 - Syringomyelia
From NCATS Genetic and Rare Diseases Information Center - [The analysis of the SpI (1546G>T) polymorphism of the Col1A1 gene and the FokI (3663T>C) polymorphism of the vitamin D receptor gene in patients with syringomyelia].
Abulgatina A S, et al. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova / Ministerstvo zdravookhraneniia i meditsinsko? promyshlennosti Rossi?sko? Federatsii, Vserossi?skoe obshchestvo nevrologov [i] Vserossi?skoe obshchestvo psikhiatrov 2007 0 (9) 60-6
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 19, 2024
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