Cutis Laxa
What's New
Last Posted: Aug 21, 2023
- ATP6V1A variants are associated with childhood epilepsy with favorable outcome.
Bin Li, et al. Seizure 2023 0 - Molecular Genetics and Pathogenesis of Ehlers-Danlos Syndrome and Related Connective Tissue Disorders.
Ritelli Marco et al. Genes 2020 May 11(5) - Whole exome sequencing analysis in severe chronic obstructive pulmonary disease.
Qiao Dandi, et al. Human molecular genetics 2018 7 - Cutis laxa
From NCATS Genetic and Rare Diseases Information Center - Cutis laxa osteoporosis
From NCATS Genetic and Rare Diseases Information Center - Cutis laxa, autosomal dominant
From NCATS Genetic and Rare Diseases Information Center - Cutis laxa, autosomal recessive type 1
From NCATS Genetic and Rare Diseases Information Center - Cutis laxa, autosomal recessive type 2A
From NCATS Genetic and Rare Diseases Information Center - Cutis laxa, autosomal recessive type 2B
From NCATS Genetic and Rare Diseases Information Center - Analysis of exonic elastin variants in severe, early-onset chronic obstructive pulmonary disease.
Cho Michael H, et al. American journal of respiratory cell and molecular biology 2009 6 (6) 751-5
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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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