Spastic Paraplegia 6
What's New
Last Posted: Jul 11, 2019
- To treat their babys rare disorder, the only case of its kind in Canada, a family risks all for a gene-therapy breakthrough
M Devlin, Globe and Mail, July 9, 2019 - Hereditary spastic paraplegia
From NCATS Genetic and Rare Diseases Information Center - Spastic paraplegia 1
From NCATS Genetic and Rare Diseases Information Center - Spastic paraplegia 10
From NCATS Genetic and Rare Diseases Information Center - Spastic paraplegia 12
From NCATS Genetic and Rare Diseases Information Center - Spastic paraplegia 13
From NCATS Genetic and Rare Diseases Information Center - Spastic paraplegia 14
From NCATS Genetic and Rare Diseases Information Center - Spastic paraplegia 15
From NCATS Genetic and Rare Diseases Information Center - Spastic paraplegia 16
From NCATS Genetic and Rare Diseases Information Center - Spastic paraplegia 19
From NCATS Genetic and Rare Diseases Information Center - Spastic paraplegia 24
From NCATS Genetic and Rare Diseases Information Center - Spastic paraplegia 25
From NCATS Genetic and Rare Diseases Information Center - Spastic paraplegia 26
From NCATS Genetic and Rare Diseases Information Center - Spastic paraplegia 29
From NCATS Genetic and Rare Diseases Information Center - Spastic paraplegia 3
From NCATS Genetic and Rare Diseases Information Center - Spastic paraplegia 31
From NCATS Genetic and Rare Diseases Information Center - Spastic paraplegia 32
From NCATS Genetic and Rare Diseases Information Center - Spastic paraplegia 51
From NCATS Genetic and Rare Diseases Information Center - Spastic paraplegia 8
From NCATS Genetic and Rare Diseases Information Center - Spastic paraplegia 9
From NCATS Genetic and Rare Diseases Information Center
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About Rare Diseases PHGKB
Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
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
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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